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This Proposed Indication Includes Patients With Locally Advanced Unresectable Nsclc Not Amenable For Definitive Chemoradiotherapy, Or Metastatic Nsclc.","dt_closure_dt":"31-JAN-2025","str_man_unit_name":"Roche Products (India) Private Limited"},{"str_drug_name":"Atezolizumab Injection","str_composition":"Atezolizumab 840.0000 Mg Per Vial","str_indication":"Atezolizumab As A Monotherapy For The First-Line Treatment Of Adult Patients With Non-Small Cell Lung Cancer (Nsclc) Who Are Ineligible For Platinum-Based Chemotherapy And Who Do Not Have Egfr Mutant Or Alk-Positive Disease. This Proposed Indication Includes Patients With Locally Advanced Unresectable Nsclc Not Amenable For Definitive Chemoradiotherapy, Or Metastatic Nsclc.","dt_closure_dt":"31-JAN-2025","str_man_unit_name":"Roche Products (India) Private Limited"},{"str_drug_name":"Atezolizumab Injection [1875mg/15ml Solution For Injection]","str_composition":"Atezolizumab 1875.0000 Mg Per Vial,Rhuph20 30000.0000 U Per Vial,L-Histidine 46.5000 Mg Per Vial,Acetic Acid, 30% 0.0000 To Ph 5.8 (Q.S.) Per Vial,Sucrose 1232.0000 Mg Per Vial,Polysorbate 20 9.0000 Mg Per Vial,L-Methionine 22.4000 Mg Per Vial,Water For Injection 0.0000 To 15ml (Q.S.) Per Vial","str_indication":"Urothelial Carcinoma Atezolizumab Is Indicated For The Treatment Of Adult Patients With Locally Advanced Or Metastatic Urothelial Carcinoma Who: ? Are Not Eligible For Cisplatin- Containing Chemotherapy And Whose Tumors Express Pd-L1 (Pd-L1 Stained Tumor-In?ltrating Immune Cells [Ic] Covering ? 5% Of The Tumor Area), As  Approved Test Or ? 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C) In Combination With Radiation Therapy For The Treatment Of  Patients With Locally Advanced Squamous Cell Cancer Of The  Head And Neck.","dt_closure_dt":"23-DEC-2025","str_man_unit_name":"M/s Merck Specialities Private Limited"},{"str_drug_name":"Cetuximab (Rdna Origin) Solution For Intravenous Infusion In Vial","str_composition":"Glycine 7.5070 Mg/Ml,Polysorbate 80 0.1000 Mg/Ml,Sodium Chloride 5.8440 Mg/Ml,Cetuximab Drug Substance (Rdna Origin) 5.0000 Mg/Ml,Sodium Hydroxide (1m) Q.S To 5.5000 Ph,Citric Acid Monohydrate 2.1010 Mg/Ml,Water For Injection Q.S To 1.0000 Ml","str_indication":"1.\tTreatment Of Patients With Squamous Cell Cancer Of The Head And Neck In Combination With Radiation Therapy For Locally Advanced Disease.,2.\tTreatment Of Patients With Epidermal Growth Factor Receptor (Egfr)- Expressing, Ras Wild-Type Metastatic Colorectal Cancer In Combination With Irinotecan-Based Chemotherapy.,3.\tTreatment Of Patients With Epidermal Growth Factor Receptor (Egfr)- Expressing, Ras Wild-Type Metastatic Colorectal Cancer In First-Line In Combination With Folfox.,4.\tTreatment Of Patients With Epidermal Growth Factor Receptor (Egfr)- Expressing, Ras Wild-Type Metastatic Colorectal Cancer As A Single Agent In Patients Who Have Failed Oxaliplatin- And Irinotecan-Based Therapy And Who Are Intolerant To Irinotecan.,5. 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For The Treatment Of Chronic Iron Overload In Patients With Non-Transfusion Dependent Thalassemia Syndromes Aged 10 Years And Older.","dt_closure_dt":"10-JUN-2019","str_man_unit_name":"Sun Pharma Laboratories Limited"},{"str_drug_name":"Deflazacort Oral Suspension (6mg/5ml) (New dosage form)","str_composition":"","str_indication":"For asthma, rheumatoid arthritis when glucocorticosteriod therapy is warranted.","dt_closure_dt":"15.06.07","str_man_unit_name":""},{"str_drug_name":"Deflazacort Tablet 18mg (Additional Strength)","str_composition":"","str_indication":"Same as approved","dt_closure_dt":"30.01.10","str_man_unit_name":""},{"str_drug_name":"Deflazocort 24mg tablets (Additional strength)","str_composition":"","str_indication":"Same as Approved.","dt_closure_dt":"14.05.08","str_man_unit_name":""},{"str_drug_name":"Deflazocort oral suspension (6mg/5ml) (new Dosage Form)","str_composition":"","str_indication":"As approved","dt_closure_dt":"15.06.07","str_man_unit_name":""},{"str_drug_name":"Deflazocort tablets","str_composition":"Each tablet contains; deflazocort-1mg,6mg,30mg","str_indication":"By specialists only- for the treatment of asthma, rheumatoid arthritis when glucocorticosteroid therapy is warranted.","dt_closure_dt":"02/11/2004","str_man_unit_name":"Macleods pharma"},{"str_drug_name":"Degarelix for Injection 80mg / 120mg per vial","str_composition":"Each pack contains; 1. One vial containing; degarelix (as acetate) 80mg, 120mg      2. One solvent vial of water for injection 6ml   3.One syringe     4. One reconstitution needle & one injection needle.","str_indication":"For the treatment of adult patients with advanced hormone dependent prostate cancer.","dt_closure_dt":"19.01.12","str_man_unit_name":"Ferring pharma"},{"str_drug_name":"Dehydrated Human Amnion Chorion Allogtaft With Phmb","str_composition":"Tissue Human Amnion Chorion Membrane Dehydrated 2.2000 Sq Cm,Polyhexamethylene Biguanide 0.5000 %","str_indication":"Intended For Use In The Treatment Of Acute And Chronic Partial And Full Thickness Wounds To Modulate Inflammation, Enhance Healing And Reduce Scar Tissue Formation,Amnionchorion Tissue Allograft With Phmb May Be Used As A Covering For Interior Or Exterior Wounds Including Use As A Covering For The Surgical Site","dt_closure_dt":"15-NOV-2022","str_man_unit_name":"LIFECELL INTERNATIONAL PRIVATE LIMITED"},{"str_drug_name":"Dehydrated Human Amnion Chorion Allogtaft With Phmb","str_composition":"Tissue Human Amnion Chorion Membrane Dehydrated 12.6000 Sq Cm,Polyhexamethylene Biguanide 0.5000 %","str_indication":"Intended For Use In The Treatment Of Acute And Chronic Partial And Full Thickness Wounds To Modulate Inflammation, Enhance Healing And Reduce Scar Tissue Formation,Amnionchorion Tissue Allograft With Phmb May Be Used As A Covering For Interior Or Exterior Wounds Including Use As A Covering For The Surgical Site","dt_closure_dt":"15-NOV-2022","str_man_unit_name":"LIFECELL INTERNATIONAL PRIVATE LIMITED"},{"str_drug_name":"Dehydro-emetine","str_composition":"","str_indication":"Anti-emetine (synthetic).","dt_closure_dt":"1963- April","str_man_unit_name":"Roche products, Bombay"},{"str_drug_name":"Delamanid Dispersible Tablets 25 Mg","str_composition":"Delamanid 25.0000 Milligram (Mg)","str_indication":"For Use As Part Of Appropriate Combination Regimen For Pulmonary Multidrug Resistant Tuberculosis Mdrtb  In Adults, Adolescents,  Children And Infants With A Body Weight Of  Atleast 10 Kg When An Effective Treatment Regimen Cannot Otherwise Be Composed For Reasons Of Resistance And Tolerability","dt_closure_dt":"19-APR-2023","str_man_unit_name":"MYLAN PHARMACEUTICALS PRIVATE LIMITED"},{"str_drug_name":"Delamanid Spray-Dried Powder","str_composition":"Delamanid 110.0000 %,Sfo67121 0.1000 %","str_indication":"NA","dt_closure_dt":"12-JAN-2021","str_man_unit_name":"Mylan Laboratories Limited"},{"str_drug_name":"Delamanid Tablets 50mg","str_composition":"Delamanid Spray Dried Powder 50.0000 Milligram (Mg)","str_indication":"Indicated For Use As Part Of An Appropriate Combination Regimen For Pulmonary Multi-Drug Resistant Tuberculosis (Mor-Tb) In Adult Patients When An Effective Treatment Regimen Cannot Otherwise Be Composed For Reasons Of Resistance Or Tolerability,In Exceptional Cases And After A Careful Benefit/Risk Assessment Delamanid Treatment Can Be Initiated In Children > 6 Years Of Age, For Use As Part Of An Appropriate Combination Regimen For Pulmonary Multi-Drug Resistant Tuberculosis (Mdr-Tb) When An Effective Treatment Regimen Cannot Otherwise Be Composed For Reasons Of Resistance Or Tolerability","dt_closure_dt":"04-MAY-2021","str_man_unit_name":"Mylan Laboratories Limited"},{"str_drug_name":"Deltamethrin (0.50% m/v) and Piperonyl Butoxide  (2.0% m/v) per ml Pour�??On Solution","str_composition":"","str_indication":"Ready to use pour-on for cattle, sheep and goats. 1. For use in Cattle to control ticks, stable flies, horn flies, cattle louse flies and nuisance flies e.g. house flies, to kill lice and protection against blackflies. 2. For use in sheep and goats for coޡ\u0005","dt_closure_dt":"29.10.09","str_man_unit_name":""},{"str_drug_name":"Deltamethrin and Piperonyl butoxide pour-on solution","str_composition":"Each ml of solution contains; deltamethrin 0.50% m/v, piperonyl butoxide-2.0% m/v","str_indication":"Ready to use pour-on for cattle, sheep and goats. For use in cattle to control ticks, stable flies, horn flies, cattle louse flies and nuisance flies e.g, house flies, to kill lice and protection against blackflies. 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House Dust Mite Allergic Asthma Not Well Controlled By Inhaled Corticosteroids And Associated With Mild To Severe House Dust Mite Allergic Rhinitis. Patients' Asthma Status Should Be Carefully Evaluated Before The Initiation Of Treatment.,Sensimune Is Indicated In Adolescents (12-17 Years) Diagnosed By Clinical History And A Positive Test Of House Dust Mite Sensitisation (Skin Prick Test And/Or Specific Ige) With Persistent Moderate To Severe House Dust Mite Allergic Rhinitis Despite Use Of Symptom-Relieving Medication.","dt_closure_dt":"28-NOV-2024","str_man_unit_name":"Dr Reddys Laboratories Limited"},{"str_drug_name":"Desamino-oxytocin","str_composition":"","str_indication":"Indicated in the treatment of induction of labour for various reasons for adequate uterine action.","dt_closure_dt":"1974- December","str_man_unit_name":"Sandoz (I) Ltd"},{"str_drug_name":"Desflurane liquid for inhalation (240mg/bottle)","str_composition":"","str_indication":"For induction & maintenance of anaesthesia.","dt_closure_dt":"22/02/2006","str_man_unit_name":""},{"str_drug_name":"Desidustat","str_composition":"Desidustat 50.0000 Milligram (Mg)","str_indication":"Treatment Of Anemia In Adult Patients With Chronic Kidney Disease (Ckd) Not On Dialysis And On Dialysis","dt_closure_dt":"07-DEC-2022","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Desidustat","str_composition":"Desidustat 25.0000 Milligram (Mg)","str_indication":"Treatment Of Anemia In Adult Patients With Chronic Kidney Disease (Ckd) Not On Dialysis And On Dialysis","dt_closure_dt":"07-DEC-2022","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Desidustat","str_composition":"Desidustat 0.0000 Milligram (Mg)","str_indication":"NA","dt_closure_dt":"07-DEC-2022","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Desidustat","str_composition":"Desidustat 100.0000 Milligram (Mg)","str_indication":"Treatment Of Anemia In Adult Patients With Chronic Kidney Disease (Ckd) Not On Dialysis And On Dialysis","dt_closure_dt":"23-NOV-2022","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Desidustat, Desidustat, Desidustat, ","str_composition":"NA","str_indication":"NA","dt_closure_dt":"07-DEC-2022","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Desloratadine (2.5mg) + Ambroxol (30mg) + Guiphenasine (50mg) + Menthol 1mg/5ml Syrup","str_composition":"","str_indication":"For productive cough.","dt_closure_dt":"02/03/2005","str_man_unit_name":""},{"str_drug_name":"Desloratadine bulk & tabs.","str_composition":"Each tab contains (film coated); desloratadine-5mg","str_indication":"Seasonal allergic rhinitis in adults.","dt_closure_dt":"30-10-2001","str_man_unit_name":"Sun pharma ltd."},{"str_drug_name":"Desloratadine + Pseudoephedrine (SR) tablets","str_composition":"Each tablet contains; desloratadine-2.5mg,5mg, pseudoephedrine SR-120mg,180mg","str_indication":"","dt_closure_dt":"2004","str_man_unit_name":"Sun, Ajanta"},{"str_drug_name":"Desloratadine tabs.","str_composition":"Each tablets 5mg desloratadine","str_indication":"For additional indication; chronic idiopathic urticaria","dt_closure_dt":"14-01-2002","str_man_unit_name":"Sun pharma"},{"str_drug_name":"Desmopressin Acetate tablet 0.1/0.2 mg","str_composition":"","str_indication":"For the treatment of cranial diabetes insipidus , primary noctumal enuresis in patients.","dt_closure_dt":"12.12.08","str_man_unit_name":""},{"str_drug_name":"Desmopressin intranasal solution/nasal solution/nasal spray/injection","str_composition":"","str_indication":"Central or neurogenic diabetes insipidus, bleeding disorders nocturnal enuresis.","dt_closure_dt":"1989-August","str_man_unit_name":"Hemm* Pharma"},{"str_drug_name":"Desmoprission lyophilisate Oral tablets 60mcg/120mcg/240mcg per tablets","str_composition":"","str_indication":"For diabetes insipidus and noctural emuresis.","dt_closure_dt":"08.05.08","str_man_unit_name":""},{"str_drug_name":"Desogestrel","str_composition":"","str_indication":"Oral contraceptive- To be used in combination with ethinyloestradiol for contraception indicated in the treatment of gastric & duodenal ulcers.","dt_closure_dt":"1989-January","str_man_unit_name":"Infar, Calcutta"},{"str_drug_name":"Desogestrel + ethinyl estradiol","str_composition":"Each pack of 22 tabs consists of 7 blue tabs of desogestrel-0.025mg, EE-0.04mg, 15 white tabs of desogestrel-0.125mg, EE-0.03mg","str_indication":"For oral contraceptive in women only","dt_closure_dt":"29-05-2000","str_man_unit_name":"Infar India ltd."},{"str_drug_name":"Desogestrel + Ethinyloestradiol tablets","str_composition":"Each tablet contains; desogestrel-0.1mg, ethinyloestradiol-0.03mg","str_indication":"","dt_closure_dt":"1983-November","str_man_unit_name":"Infar, Calcutta"},{"str_drug_name":"Desogestrel tab","str_composition":"Each film coated tab contains; desogestrel-0.075mg","str_indication":"Oral contraception in women only","dt_closure_dt":"20-08-2002","str_man_unit_name":"Infon India ltd."},{"str_drug_name":"Desonide","str_composition":"Single Unknown Impurity 0.1000 %,16a-Hydroxyprednisolone (Imp A Usp) 0.1500 %,Assay 98.0000 %,Delta 9,11 Desonide 0.1000 %,Desonide 21-Acetate (Imp H Usp) 0.1500 %,Desonide 21-Aldehyde (Imp C Usp) 0.3000 %,Desonide 9,11-Epoxide (Imp F Usp) 0.1500 %,Sum Of Dihydrodesonide Delta 16 Prednisolone 0.4000 %,Total Impurities 1.0000 %,1,2-Dihydro Desonide (Imp E Usp) 0.2500 %,Prednisolone (Imp B Usp) 0.1000 %,Delta 16 Prednisolone (Imp D Usp) 0.1000 %,Sum Desonide Aldehyde And Delta 16 Prednisolone 0.4000 %,9a Bromo Desonide 0.1000 %","str_indication":"NA","dt_closure_dt":"30-DEC-2022","str_man_unit_name":"G. Loucatos& Co."},{"str_drug_name":"Desonide cream","str_composition":"Desonide cream-0.05%","str_indication":"For relief of the inflammatory and pruritic manifestation of corticosteroid responsive dermatosis.","dt_closure_dt":"07/03/1997","str_man_unit_name":"Crosland research"},{"str_drug_name":"Desonide Ointment 0.05%","str_composition":"Desonide 0.0500 Weight/Weight(W/W),Desonide-21-Aldehyde Hydrate (Impurity-C) 1.0000 Weight/Weight(W/W),Any Individual Unspecified Impurity 0.5000 Weight/Weight(W/W),Total Impurities 2.0000 Weight/Weight(W/W)","str_indication":"Anti Inflammatory,Anti-Pruritic,Dermatosis","dt_closure_dt":"27-SEP-2019","str_man_unit_name":"ENCUBE ETHICALS PVT. LTD"},{"str_drug_name":"Desoximetasone","str_composition":"","str_indication":"Topical corticosteroid- Indicated in the management of various acute and chronic dermatoses viz eczema, nummular eczema, infantile eczema, atopical dermatitis.","dt_closure_dt":"1975-July","str_man_unit_name":"Hoechst, Bombay"},{"str_drug_name":"Desoximetasone","str_composition":"Each 1 gm contains; Desoximetasone-2.5mg","str_indication":"Topical corticosteroid- Indicated in the management of various acute and chronic dermatoses viz eczema, nummular eczema, infantile eczema, atopical dermatitis.","dt_closure_dt":"1975-September","str_man_unit_name":"Hoechst, Bombay"},{"str_drug_name":"Desoximetasone 0.05% oitment","str_composition":"Desoximetasone-0.05%","str_indication":"","dt_closure_dt":"1979-July","str_man_unit_name":"Hoechst"},{"str_drug_name":"Desvenlafaxine (as Succinate) ER Tablets  50mg/100mg","str_composition":"Each uncoated ER tablet contains; desvenlafaxine succinate eq.to desvenlafaxine-50mg, 100mg","str_indication":"For the treatment of major depressive disorder (MDD).","dt_closure_dt":"20.07.09","str_man_unit_name":"Intas pharma, Ahmedabad, Cadila healthcare ltd., Sun pharma"},{"str_drug_name":"Dexamethasone + indomethacin","str_composition":"Each capsule contains; Dexamethasone-0.125 mg, indomethacin-25 mg","str_indication":"","dt_closure_dt":"1971- November","str_man_unit_name":"MSD, Bombay"},{"str_drug_name":"Dexamethasone Intravitreal Implant","str_composition":"Dexamethasone 0.7000 Milligram (Mg)","str_indication":"Ozurdex� Is Indicated For The Treatment Of Diabetic Macular Edema","dt_closure_dt":"15-JUN-2022","str_man_unit_name":"AbbVie Therapeutics India Private Limited"},{"str_drug_name":"Dexamethasone Intravitreal implant 0.7mg (Additional Indication)","str_composition":"","str_indication":"For the treatment of visual impairment due to Diabetic Macular Edema (DME) who are pseudophakic or who are considered insufficiently responsive to, or unsuitable for non-corticosteroid therapy.","dt_closure_dt":"12.10.15","str_man_unit_name":""},{"str_drug_name":"Dexamethasone Intravitreal Implant 0.7mg (in solid polymer drug delivery system)","str_composition":"","str_indication":"For the treatment of non-infectious uveitis affecting the posterior segment of the eye. However it should not be used when there is gap in posterior capsule.","dt_closure_dt":"20.02.13","str_man_unit_name":""},{"str_drug_name":"Dexamethasone Intravitreal Implant 0.7mg (in solid polymer drug delivery system)","str_composition":"","str_indication":"For the treatment of macular edema following branch retinal vein occlusion (CRVO).","dt_closure_dt":"16.01.10","str_man_unit_name":""},{"str_drug_name":"Dexamethasone Metasulfobenzoate Sodium","str_composition":"Dexamethasone Metasulfobenzoate Sodium 0.0000 Gram (G)","str_indication":"NA","dt_closure_dt":"13-DEC-2021","str_man_unit_name":"Sanofi India Limited"},{"str_drug_name":"Dexamethasone sodium metasulphobenzoate","str_composition":"","str_indication":"Corticosteroid, anti-inflammatory.","dt_closure_dt":"1962- April","str_man_unit_name":"Khandelwal, Bombay"},{"str_drug_name":"Dexamethasone tablets","str_composition":"Each uncoated tablet contains; dexamethasone IP-4mg,8mg","str_indication":"Oncologists only- for steroid responsive neoplastic disease like leukemias and lymphomas in adults only.","dt_closure_dt":"02/11/2004","str_man_unit_name":"Sun pharma, Dr. Reddy"},{"str_drug_name":"Dexamethasone Tablets Ip","str_composition":"Dexamethasone 2.0000 Milligram (Mg)","str_indication":"Indicated For Treatment Of Variety Of Disorders In Which Systemic Glucocorticoids Are Indictaed. For Details Refer The Indcation Section Of Prescribing Information .","dt_closure_dt":"05-APR-2021","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Dexamethasone Tablets Ip","str_composition":"Dexamethasone 6.0000 Milligram (Mg)","str_indication":"Indicated For Treatment Of Variety Of Disorders In Which Systemic Glucocorticoids Are Indictaed. For Details Refer The Indcation Section Of Prescribing Information .","dt_closure_dt":"05-APR-2021","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Dexamethasone trimethyl acetate","str_composition":"","str_indication":"New salt for topical formulation.","dt_closure_dt":"1961- August","str_man_unit_name":"Ciba Pharma"},{"str_drug_name":"Dexchlorpheniramine maleate","str_composition":"Each tablet contains; Dexchlorpheniramine maleate-2mg","str_indication":"","dt_closure_dt":"1976-July","str_man_unit_name":"Micro Labs, Madras"},{"str_drug_name":"Dexfenfluramine hcl. 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Ii) Maintaining healing of EE and relief of heartburn. 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Dexmedetomidine Rtu Should Be Administered By Continuous Infusion Not To Exceed 24 Hours. It Has Been Continuously Infused In Mechanically Ventilated Adult Patients Prior To Extubation, During Extubation, And Post-Extubation.","dt_closure_dt":"18-NOV-2025","str_man_unit_name":"Amneal Pharmaceuticals Pvt.Ltd."},{"str_drug_name":"Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride Injection, 4 Mcg/Ml (200 Mcg/50 Ml And 400 Mcg/100 Ml)","str_composition":"Dexmedetomidine Hydrochloride Equivalent To Dexmedetomidine 4.0000 Mcg/Ml (400 Mcg/100 Ml)","str_indication":"Indicated For Sedation Of Initially Intubated And Mechanically Ventilated Adult Patients During Treatment In An Intensive Care Setting. Dexmedetomidine Rtu Should Be Administered By Continuous Infusion Not To Exceed 24 Hours. It Has Been Continuously Infused In Mechanically Ventilated Adult Patients Prior To Extubation, During Extubation, And Post-Extubation.","dt_closure_dt":"18-NOV-2025","str_man_unit_name":"Amneal Pharmaceuticals Pvt.Ltd."},{"str_drug_name":"Dexrabeprazole 10mg (EC) + Domperidone 30mg SR Capsules","str_composition":"","str_indication":"For the treatment of Gastroeasophageal Reflux Disease (GERD) in patients not responding to dexrabeprazole alone.","dt_closure_dt":"09.06.08","str_man_unit_name":""},{"str_drug_name":"Dexrabeprazole Sodium E. 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To 0.5000 Ml","str_indication":"Indicated For Primary Immunization Against Diphtheria, Tetanus, Pertussis, Hepatitis B, And Invasive Diseases Caused By Haemophilus Influenzae Type B From The Age Of 6 Weeks Onwards, In Accordance With Official Recommendations","dt_closure_dt":"28-OCT-2021","str_man_unit_name":"Sanofi Healthcare India Private Limited"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis B (Rdna) And Haemophilus Influenzae Type B Conjugate Vaccine (Adsorbed) I.P.","str_composition":"Diphtheria Toxoid 20.0000 Lf To <= 30 Lf (>= 2.0 Units/Ml),Tetanus Toxoid 5.0000 Lf To < 25 Lf (>= 60.0 Iu),B. Pertussis 4.0000 Iu,Hbsag (Rdna) 10.0000 Micrograms (?g),Purified Capsular Polysaccharide (Prp) ?  Conjugated To Tetanus Toxoid (Carrier Protein) 10.0000 ?g  (19 To 33 ?g),Aluminium (Al3+) (As Aluminium Phosphate Gel) 1.2500 Milligram (Mg),2-Phenoxyethanol 2.5000 Milligram (Mg)","str_indication":"It Is Indicated For The Active Immunization Of Infants, At Or Above The Age Of 6 Weeks Against Diphtheria, Tetanus, Whooping Cough, Hepatitis B And Haemophilus Influenzae Type B Infections.","dt_closure_dt":"22-JUN-2020","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis-B (Rdna) And Haemophilus Influenza Type-B Conjugate Vaccine (Adsorbed)- Ready To Fill Bulk","str_composition":"Diphtheria Toxoid 30.0000 Iu,Tetanus Toxoid 60.0000 Iu,Inactivated Whole Cell Bordetella Pertussis 4.0000 Iu,Hepatitis B Surface Antigen (Rdna) 10.0000 Micrograms (?g),Hib Polysaccharide Covalently Bound To Tt (Prp-Tt) 10.0000 Micrograms (?g),Al +++ Content (As Alpo 4 Gel) 1.2500 Milligram (Mg),Thiomersal (As Preservative) 0.0100 % W/V,Normal Saline (Sodium Chloride 0.9%) 0.0000 Q.S. To 0.5 Ml","str_indication":"NA","dt_closure_dt":"16-MAY-2025","str_man_unit_name":"INDIAN IMMUNOLOGICAL LIMITED"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis B (Rdna), Haemophilus Influenzae Type B Conjugate And Poliomyelitis (Inactivated) (Adsorbed) Final Bulk Vaccine [Ready To Fill Mono-Dose]","str_composition":"Tetanus Toxoid 60.0000 Iu,Poliomyelitis Virus (Inactivated) Type 3 (Saukett Strain) 32.0000 Du Or Equivalent Quantity By Immunochemical Method,Rdna Hepatitis B Surface Antigen 10.0000 Micrograms (?g),Poliomyelitis Virus (Inactivated) Type 1 (Mahoney Strain) 40.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 2 (Mef-1 Strain) 8.0000 Du Or Equivalent Quantity By Immunochemical Method,Water For Injections Q.S. To 0.5000 Ml,Aluminium Phosphate Gel Equivalent To Al +++ 0.6250 Milligram (Mg),Diphtheria Toxoid 30.0000 Iu,Bordetella Pertussis (Whole Cell Inactivated) 4.0000 Iu,Haemophilus Influenzae Type B Polysaccharide (Prp) Conjugated To Tetanus Toxoid 22 To 40 ?g 12.0000 Micrograms (?g),Sodium Chloride 4.5000 Milligram (Mg)","str_indication":"NA","dt_closure_dt":"07-OCT-2021","str_man_unit_name":"Sanofi Healthcare India Private Limited"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis B (Rdna), Haemophilus Influenzae Type B Conjugate And Poliomyelitis (Inactivated) (Adsorbed) Final Bulk Vaccine [Ready To Fill Multi-Dose]","str_composition":"Diphtheria Toxoid 30.0000 Iu,Tetanus Toxoid 60.0000 Iu,Bordetella Pertussis (Whole Cell Inactivated) 4.0000 Iu,Rdna Hepatitis B Surface Antigen 10.0000 Micrograms (?g),Haemophilus Influenzae Type B Polysaccharide (Prp) Conjugated To Tetanus Toxoid 22 To 40 ?g 12.0000 Micrograms (?g),Poliomyelitis Virus (Inactivated) Type 1 (Mahoney Strain) 40.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 2 (Mef-1 Strain) 8.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 3 (Saukett Strain) 32.0000 Du Or Equivalent Quantity By Immunochemical Method,Aluminium Phosphate Gel Equivalent To Al +++ 0.6250 Milligram (Mg),Sodium Chloride 4.5000 Milligram (Mg),2-Phenoxyethanol 0.6000 %V/V,Formaldehyde 6.2500 Micrograms (?g),Water For Injections Q.S. To 0.5000 Ml","str_indication":"NA","dt_closure_dt":"18-OCT-2021","str_man_unit_name":"Sanofi Healthcare India Private Limited"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis B (Rdna), Haemophilus Influenzae Type B Conjugate And Poliomyelitis (Inactivated) Vaccine (Adsorbed).","str_composition":"Diphtheria Toxoid 30.0000 Iu,Tetanus Toxoid 60.0000 Iu,Bordetella Pertussis (Whole Cell Inactivated) 4.0000 Iu,Rdna Hepatitis B Surface Antigen 10.0000 Micrograms (?g),Haemophilus Influenzae Type B Polysaccharide (Prp) Conjugated To Tetanus Toxoid 22 To 40 ?g 12.0000 Micrograms (?g),Poliomyelitis Virus (Inactivated) Type 1 (Mahoney Strain) 40.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 2 (Mef-1 Strain) 8.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 3 (Saukett Strain) 32.0000 Du Or Equivalent Quantity By Immunochemical Method,Aluminium Phosphate Gel Equivalent To Al +++ 0.6250 Milligram (Mg),Sodium Chloride 4.5000 Milligram (Mg),2-Phenoxyethanol 0.6000 %V/V,Formaldehyde 6.2500 Micrograms (?g),Water For Injections Q.S. To 0.5000 Ml","str_indication":"Indicated For Primary And Booster Vaccination Against Diphtheria, Tetanus, Pertussis, Poliomyelitis, Hepatitis B, And Invasive Diseases Caused By Haemophilus Influenzae Type B From The Age Of 6 Weeks Onwards, In Accordance With Official Recommendations.","dt_closure_dt":"28-MAY-2021","str_man_unit_name":"Sanofi Healthcare India Private Limited"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis B (Rdna), Haemophilus Influenzae Type B Conjugate And Poliomyelitis (Inactivated) Vaccine (Adsorbed).","str_composition":"Diphtheria Toxoid 30.0000 Iu,Tetanus Toxoid 60.0000 Iu,Bordetella Pertussis (Whole Cell Inactivated) 4.0000 Iu,Rdna Hepatitis B Surface Antigen 10.0000 Micrograms (?g),Haemophilus Influenzae Type B Polysaccharide (Prp) Conjugated To Tetanus Toxoid 22 To 40 ?g 12.0000 Micrograms (?g),Poliomyelitis Virus (Inactivated) Type 1 (Mahoney Strain) 40.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 2 (Mef-1 Strain) 8.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 3 (Saukett Strain) 32.0000 Du Or Equivalent Quantity By Immunochemical Method,Aluminium Phosphate Gel Equivalent To Al +++ 0.6250 Milligram (Mg),Sodium Chloride 4.5000 Milligram (Mg),Water For Injections Q.S. To 0.5000 Ml","str_indication":"Indicated For Primary And Booster Vaccination Against Diphtheria, Tetanus, Pertussis, Poliomyelitis, Hepatitis B, And Invasive Diseases Caused By Haemophilus Influenzae Type B From The Age Of 6 Weeks Onwards, In Accordance With Official Recommendations.","dt_closure_dt":"21-MAY-2021","str_man_unit_name":"Sanofi Healthcare India Private Limited"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis B (Rdna), Haemophilus Influenzae Type B Conjugate And Poliomyelitis (Inactivated) Vaccine (Adsorbed).","str_composition":"Diphtheria Toxoid 30.0000 Iu,Tetanus Toxoid 60.0000 Iu,Bordetella Pertussis (Whole Cell Inactivated) 4.0000 Iu,Rdna Hepatitis B Surface Antigen 10.0000 Micrograms (?g),Haemophilus Influenzae Type B Polysaccharide (Prp) Conjugated To Tetanus Toxoid 22 To 40 ?g 12.0000 Micrograms (?g),Poliomyelitis Virus (Inactivated) Type 1 (Mahoney Strain) 40.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 2 (Mef-1 Strain) 8.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 3 (Saukett Strain) 32.0000 Du Or Equivalent Quantity By Immunochemical Method,Aluminium Phosphate Gel Equivalent To Al +++ 0.6250 Milligram (Mg),Sodium Chloride 4.5000 Milligram (Mg),2-Phenoxyethanol 0.6000 %V/V,Formaldehyde 6.2500 Micrograms (?g),Water For Injections Q.S. To 0.5000 Ml","str_indication":"Indicated For Primary And Booster Vaccination Against Diphtheria, Tetanus, Pertussis, Poliomyelitis, Hepatitis B, And Invasive Diseases Caused By Haemophilus Influenzae Type B From The Age Of 6 Weeks Onwards, In Accordance With Official Recommendations.","dt_closure_dt":"21-MAY-2021","str_man_unit_name":"Sanofi Healthcare India Private Limited"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis B (Rdna), Haemophilus Influenzae Type B Conjugate And Poliomyelitis (Inactivated) Vaccine (Adsorbed).","str_composition":"Diphtheria Toxoid 30.0000 Iu,Tetanus Toxoid 60.0000 Iu,Bordetella Pertussis (Whole Cell Inactivated) 4.0000 Iu,Rdna Hepatitis B Surface Antigen 10.0000 Micrograms (?g),Haemophilus Influenzae Type B Polysaccharide (Prp) Conjugated To Tetanus Toxoid 22 To 40 ?g 12.0000 Micrograms (?g),Poliomyelitis Virus (Inactivated) Type 1 (Mahoney Strain) 40.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 2 (Mef-1 Strain) 8.0000 Du Or Equivalent Quantity By Immunochemical Method,Poliomyelitis Virus (Inactivated) Type 3 (Saukett Strain) 32.0000 Du Or Equivalent Quantity By Immunochemical Method,Aluminium Phosphate Gel Equivalent To Al +++ 0.6250 Milligram (Mg),Sodium Chloride 4.5000 Milligram (Mg),Water For Injections Q.S. To 0.5000 Ml","str_indication":"Indicated For Primary And Booster Vaccination Against Diphtheria, Tetanus, Pertussis, Poliomyelitis, Hepatitis B, And Invasive Diseases Caused By Haemophilus Influenzae Type B From The Age Of 6 Weeks Onwards, In Accordance With Official Recommendations.","dt_closure_dt":"28-MAY-2021","str_man_unit_name":"Sanofi Healthcare India Private Limited"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis B (R-Dna), Inactivated Poliomyelitis And Haemophilus Influenzae Type B Conjugate Vaccine (Adsorbed) - Single Dose (0.5 Ml) And Multi Dose (2.5 Ml)","str_composition":"B. Pertussis (Whole Cell, Killed) 4.0000 Iu,Inactivated Poliomyelitis Virus Type -2 (S19/Mef2p1/N18s) 8.0000 D Antigen Units,Inactivated Poliomyelitis Virus Type -1 (S19/Mahp1/N18s) 40.0000 D Antigen Units,Diphtheria Toxoid 30.0000 Iu,R-Hbsag (Recombinant Hbs Antigen Produced In Pichia Pastoris) 12.5000 Milligram (Mg),Tetanus Toxoid 60.0000 Iu,Purified Capsular Polysaccharide Of Hib (Prp) Covalently Linked To 20 To 36.7 ?g Of Tetanus Toxoid 11.0000 Micrograms (?g),Inactivated Poliomyelitis Virus Type -3 (S19/Sktp1/N18s) 32.0000 D Antigen Units,2-Phenoxyethanol 4.0000 Milligram (Mg),Al+++ (As Alpo4) 1.2500 Milligram (Mg)","str_indication":"For Active Immunization To Prevent Diphtheria, Tetanus, Pertussis, Hepatitis B, Poliomyelitis Types 1, 2, 3 And Haemophilus Influenzae Type B","dt_closure_dt":"07-MAY-2026","str_man_unit_name":"Biological E - Shameerpet"},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis-B (Rdna), Poliomyelitis (Inactivated) And Haemophilus Influenzae Type B Conjugate Vaccine (Adsorbed)","str_composition":"Diphtheria Toxoid 30.0000 Iu,Tetanus Toxoid 40.0000 Iu,Bordetella Pertussis (Whole Cell) 4.0000 Iu,Hepatitis B Surface Antigen (Rdna) 15.0000 Micrograms (?g),Inactivated Polio Vaccine (Grown On Salk Strain Of Vero Cells)  Type -1 (Mahoney Strain) 40.0000 Du,Inactivated Polio Vaccine (Grown On Salk Strain Of Vero Cells) Type -2 (Mef-1 Strain) 8.0000 Du,Inactivated Polio Vaccine (Grown On Salk Strain Of Vero Cells) Type -3 (Saukett Strain) 32.0000 Du,Haemophilus Influenzae Type B (Prp) Conjugated To Tetanus Toxoid (Carrier Protein) 10.0000 Mcg (19 To 33 Mcg),Aluminium Content Al +++ (As Aluminium Phosphate Gel) 1.2500 Milligram (Mg),2-Phenoxyethanol 0.5000 %","str_indication":"Hexasiil Is Indicated For Primary And Booster Vaccination Of Infants And Toddlers From Six Weeks Of Age Against  Diphtheria, Tetanus, Pertussis, Hepatitis B, Poliomyelitis And Invasive Diseases Caused By Haemophilus Influenzae Type  B","dt_closure_dt":"14-SEP-2022","str_man_unit_name":"SERUM INSTITUTE OF INDIA PVT. LTD."},{"str_drug_name":"Diphtheria, Tetanus, Pertussis (Whole Cell), Hepatitis B (Rdna), Poliomyelitis (Inactivated) And Haemophilus Influenzae Type B Conjugate Vaccine (Adsorbed), Ready To Fill Bulk.","str_composition":"Diphtheria Toxoid 30.0000 Iu,Tetanus Toxoid 40.0000 Iu,Bordetella Pertussis (Whole Cell) 4.0000 Iu,Hepatitis B Surface Antigen (Rdna) 15.0000 Micrograms (?g),Inactivated Polio Vaccine (Salk Strains Grown On Vero Cells) Type- 1 (Mahoney Strain) 40.0000 Du,Inactivated Polio Vaccine (Salk Strains Grown On Vero Cells) Type- 2 (Mef-1 Strain) 8.0000 Du,Inactivated Polio Vaccine (Salk Strains Grown On Vero Cells) Type- 3 (Saukett Strain) 32.0000 Du,Haemophilus Influenzae Type B (Prp)Conjugated To Tetanus Toxoid (Carrier Protein) 10.0000 Mcg (19 To 33 Mcg),Aluminium Content Al+++ (As Aluminium Phosphate Gel) 1.2500 Milligram (Mg),2-Phenoxyethanol 0.5000 %","str_indication":"NA","dt_closure_dt":"17-JAN-2024","str_man_unit_name":"SERUM INSTITUTE OF INDIA PVT. LTD."},{"str_drug_name":"Diphtheria Toxoid Bulk (Thiomersal?Free)","str_composition":"Diphtheria Toxoid Bulk (Thiomersal?Free) 2000.0000 Lf/Ml","str_indication":"NA","dt_closure_dt":"15-MAY-2026","str_man_unit_name":"Biological E - Shameerpet"},{"str_drug_name":"Dipiprolate","str_composition":"Dragee-40mg","str_indication":"Anti-tussive.","dt_closure_dt":"1964- March","str_man_unit_name":"Hoechlin, Bombay"},{"str_drug_name":"Dipivefrin hcl ophthalmic solution USP","str_composition":"Dipivefrin hcl USP-0.1%","str_indication":"For the control of intra-ocular pressure in chronic open angle glaucoma.","dt_closure_dt":"16/05/1996","str_man_unit_name":"Nicholas piramal"},{"str_drug_name":"Diptheria + tetanus toxoid + pertusis vaccine adsorbed & haemophilus bCRM197. conjugated vacc.","str_composition":"","str_indication":"For active immunization of children (2 months-5 years) against diptheria, tetanus, pertusis & haemophilus-B diseases.","dt_closure_dt":"12/10/1999","str_man_unit_name":"Wyeth lab, Bombay"},{"str_drug_name":"Dipyridamole","str_composition":"tab-12.5mg, amp-2ml of 10mg","str_indication":"Coronary vasodilator.","dt_closure_dt":"1964- April","str_man_unit_name":"Germen remedies, Bombay"},{"str_drug_name":"Disinfectant (D-125) solution","str_composition":"Each bottle contains; n-Alkyl dimethyl benzyl ammonium chloride-2.37% and n-Alkyl dimethyl ethyl benzyl ammonium chloride-2.37%, inert ingredients-95.26%","str_indication":"To disinfect hard , non-porous surfaces against micro-organisms like E.coli, Staphylococcus and Klebseilla.","dt_closure_dt":"03.05.07","str_man_unit_name":"Microgen hygiene pvt ltd."},{"str_drug_name":"Disodium Cromoglycate","str_composition":"Disodium Cromoglycate-2%","str_indication":"","dt_closure_dt":"1976-September","str_man_unit_name":"Unique chemical, Bombay"},{"str_drug_name":"Disodium Hydrogen Phosphate Dihydrate","str_composition":"NA","str_indication":"NA","dt_closure_dt":"01-NOV-2021","str_man_unit_name":"M/s BioGenomics Limited"},{"str_drug_name":"Disodium pamidronate injection","str_composition":"","str_indication":"Tumour inducer hypercalcaemia.","dt_closure_dt":"21/02/1995","str_man_unit_name":"Hindustan ciba geigy ltd., Mac labs."},{"str_drug_name":"Disodium Phosphate Dihydrate (Solution For Haemodialysis / Haemofiltration)+Magnesium Chloride Hexahydrate+Potassium Chloride+Sodium Chloride+Sodium Hydrogen Carbonate","str_composition":"Magnesium Chloride Hexahydrate 3.0500 G/L,Sodium Chloride 7.0100 G/L,Sodium Hydrogen Carbonate 2.1200 G/L,Potassium Chloride 0.3140 G/L,Disodium Phosphate Dihydrate 0.1870 G/L","str_indication":"Biphozyl Is Used As Replacement Solution And As A Dialysate For Treatment Of Acute Kidney Injury During Continuous Renal Replacement Therapy. Biphozyl Is Used In A Post-Acute Phase After Initiation Of Renal Replacement Therapy When Therapy When Ph, Potassium And Phosphate Concentration Have Returned To Normal. Biphozyl Is Also Used When Other Buffer Sources Are Available As Well As During Regional Citrate Anticoagulation. Moreover Biphozyl Is Used In Patients With Hypercalcaemia. Biphozyl May Also Be Used In Patients With Hypercalcemia. Biphozyl May Also Be Used In Cases Of Drug Poisoning Or Intoxications When The Substance Are Dialysable Or Filterable","dt_closure_dt":"22-MAY-2020","str_man_unit_name":"Baxter India Pvt. Ltd."},{"str_drug_name":"Disodium Succinic Salt Hexahydrate","str_composition":"NA","str_indication":"NA","dt_closure_dt":"10-APR-2026","str_man_unit_name":"Dr Reddys Laboratories Limited"},{"str_drug_name":"Disophenol","str_composition":"Each c.c contains; disophenol-45mg","str_indication":"Treatment of hook worm in dogs and cats.","dt_closure_dt":"1970- April","str_man_unit_name":"Cyamid India Ltd, Bombay"},{"str_drug_name":"Disopyramide ","str_composition":"Each capsule contains; Disopyramide-100mg","str_indication":"Anti-arrhythimic agent- indicated in the treatment of cardiac arrhythmias including atrial fibrillation, vent. tachycardia arrhythmia.","dt_closure_dt":"1977-June","str_man_unit_name":"Roussel Pharma, Bombay"},{"str_drug_name":"Disopyramide injection","str_composition":"Each ampoule contains; disopyramide phosphate eq.to 100mg of disopyramide base in 5ml aqueous solution, disopyramide phosphate eq.to 150mg of disopyramide base in 7.5ml aqueous solution.","str_indication":"","dt_closure_dt":"1983-August","str_man_unit_name":"Searle"},{"str_drug_name":"Disprospan injection","str_composition":"Each vial contains; betamethasone dipropionate-6.43mg, betamethasone sodium phosphate-2.63mg","str_indication":"","dt_closure_dt":"1984-July","str_man_unit_name":"Fulford"},{"str_drug_name":"Divalproex Sodium Oral Solution 500mg/5ml (Additional Dosage Form)","str_composition":"","str_indication":"For monotherapy and adjunctive therapy in the treatment of patients with complex partial seizures that occur either in isolation or in association with types of seizures for adult patients only.","dt_closure_dt":"23.12.13","str_man_unit_name":""},{"str_drug_name":"Divalproex sodium sprinkle capsule","str_composition":"Each sprinkle capsule contains; divalproex sodium eq.to valproic acid-125mg, 250mg","str_indication":"As monotherapy and adjunctive therapy in the treatment of patients with complex partial seizures that occur either in isolation or in association with other types of seizure.","dt_closure_dt":"06.12.07","str_man_unit_name":"Torrent pharma"},{"str_drug_name":"Divalproex sodium tab","str_composition":"Each enteric coated tab contains; divalproex sodium eq.to valproic acid-125mg,250mg,500mg","str_indication":"As monotherapy or adjunctive therapy in the treatment of patients with complex partial seizure and manic episodes associated with bipolar disorder.","dt_closure_dt":"17-01-2002","str_man_unit_name":"Cadila pharma ltd."},{"str_drug_name":"Divalproex sodium tablets","str_composition":"","str_indication":"For additional prescription condition to be sold under Neurologist & Psychiatrist only.","dt_closure_dt":"21/04/2004","str_man_unit_name":"Medreich steri labs."},{"str_drug_name":"Divalproex sodium tablets","str_composition":"Extended release tablets-250mg,500mg,125mg","str_indication":"For additional indication-prphylaxis of migraine headache in adults with warning -not for women who are pregnant or planning for pregnancy.","dt_closure_dt":"2004-August","str_man_unit_name":"Sun pharma"},{"str_drug_name":"Divalproex sodium tablets","str_composition":"Each extended release tablet contains; divalproex sodium-750mg, 1000mg.","str_indication":"Additional indication- prophylaxis of migraine headache.","dt_closure_dt":"25/06/2004","str_man_unit_name":"Sun pharma"},{"str_drug_name":"dl-naorgestrel + Ethinyl oestradiol","str_composition":"Each tablet contains; dl-naorgestrel-0.5mg, Ethinyl oestradiol-0.03mg","str_indication":"Oral contraceptive ","dt_closure_dt":"1975- April","str_man_unit_name":"German Remedies Bombay"},{"str_drug_name":"dl-norgestrel + ethinyl oestradiol","str_composition":"Each tablet contains; dl-norgestrel-0.25mg, ethinyl oestradiol-0.05mg","str_indication":"Oral contraceptive","dt_closure_dt":"1971- October","str_man_unit_name":"Wyeth lab, Bombay"},{"str_drug_name":"dl-norgestrel + Ethinyloestradiol","str_composition":"Each tablet contains; dl-norgestrel-300mcg, Ethinyloestradiol-30mcg","str_indication":"","dt_closure_dt":"1976-October","str_man_unit_name":"Wyeth Labs, Bombay"},{"str_drug_name":"d-Norgestrel","str_composition":"Each tablet contains; d-Norgestrel-0.03mg","str_indication":"","dt_closure_dt":"1974- August","str_man_unit_name":"Wyeth Labs Bombay"},{"str_drug_name":"d-Norgestrel","str_composition":"Each coated tablet contains; d-Norgestrel-0.03mg","str_indication":"Oral contraceptive","dt_closure_dt":"1974-April","str_man_unit_name":"German Remedies, Bombay"},{"str_drug_name":"d-Norgestrel + Ehinyloestradiol","str_composition":"Each tablet contains; 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To Tofacitinib?.11mg/22mg","str_composition":"Tofacitinib Citrate Equ. To Tofacitinib 11.0000 Milligram (Mg)","str_indication":"Rheumatoid Arthritis: Indicated For The Treatment Of Adult Patients With Moderately To Severely Active Rheumatoid Arthritis (Ra) Who Have Had An Inadequate Response Or Intolerance To One Or More Tnf Blockers. Psoriatic Arthritis: Indicated For The Treatment Of Adult Patients With Active Psoriatic Arthritis (Psa) Who Have Had An Inadequate Response Or Intolerance To One Or More Tnf Blockers. Ulcerative Colitis: Indicated For The Treatment Of Adult Patients With Moderately To Severely Active Ulcerative Colitis (Uc), Who Have An Inadequate Response Or Intolerance To One Or More Tnf Blockers","dt_closure_dt":"09-JAN-2023","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Extended Release Tablet Contains Tofacitinib Citrate Eq. To Tofacitinib?.11mg/22mg","str_composition":"Tofacitinib Citrate Equ. To Tofacitinib 22.0000 Milligram (Mg)","str_indication":"Rheumatoid Arthritis: Indicated For The Treatment Of Adult Patients With Moderately To Severely Active Rheumatoid Arthritis (Ra) Who Have Had An Inadequate Response Or Intolerance To One Or More Tnf Blockers. Psoriatic Arthritis: Indicated For The Treatment Of Adult Patients With Active Psoriatic Arthritis (Psa) Who Have Had An Inadequate Response Or Intolerance To One Or More Tnf Blockers. Ulcerative Colitis: Indicated For The Treatment Of Adult Patients With Moderately To Severely Active Ulcerative Colitis (Uc), Who Have An Inadequate Response Or Intolerance To One Or More Tnf Blockers","dt_closure_dt":"09-JAN-2023","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Prolonged Release Tablet Contains Ivabradine Hydrochloride Eq. To Ivabradine 10mg/15mg","str_composition":"Ivabradine Hydrochloride Eq. To Ivabradine 15 Mg 15.0000 Milligram (Mg)","str_indication":"For The Treatment Of Chronic Stable Angina Pectoris In Patients With Coronary Artery Disease And Treatment Of Chronic Heart Failure.","dt_closure_dt":"28-OCT-2020","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Film Coated Prolonged Release Tablet Contains Ivabradine Hydrochloride Eq. To Ivabradine 10mg/15mg","str_composition":"Ivabradine Hydrochloride Eq. To Ivabradine 10mg 10.0000 Milligram (Mg)","str_indication":"For The Treatment Of Chronic Stable Angina Pectoris In Patients With Coronary Artery Disease And Treatment Of Chronic Heart Failure.","dt_closure_dt":"28-OCT-2020","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Film Coated Prolonged Release Tablets Contains : Mirabegron 25 Mg/50 Mg","str_composition":"Mirabegron 50.0000 Milligram (Mg)","str_indication":"Symptomatic Treatment Of Urgency, Increased Micturition Frequency And / Or Urgency Incontinence As May Occur In Patients With Over Active Bladder (Oab) Syndrome","dt_closure_dt":"03-SEP-2020","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Film Coated Prolonged Release Tablets Contains : Mirabegron 25 Mg/50 Mg","str_composition":"Mirabegron 25.0000 Milligram (Mg)","str_indication":"Symptomatic Treatment Of Urgency, Increased Micturition Frequency And / Or Urgency Incontinence As May Occur In Patients With Over Active Bladder (Oab) Syndrome","dt_closure_dt":"03-SEP-2020","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Film Coated Tablet Contains Bempedoic Acid ?.180 Mg","str_composition":"Bempedoic Acid 180.0000 Milligram (Mg)","str_indication":"It S Indicated As An Adjunct To Diet And Maximally Tolerated Statin Therapy For The  Treatment Of Adults With Heterozygous Familial Hypercholesterolemia Or Established  Atherosclerotic Cardiovascular Disease Who Require Additional Lowering Of Ldl-C","dt_closure_dt":"24-MAY-2022","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablet Contains Bempedoic Acid 180 Mg Tablets","str_composition":"Bempedoic Acid 180.0000 Milligram (Mg)","str_indication":"As An Adjunct To Diet And Maximally Tolerated Statin Therapy For The Treatment Of Adults With Heterozygous Familial Hypercholesterolemia Or Established Atherosclerotic Cardiovascular Disease Who Require Additional Lowering Of Ldl-C","dt_closure_dt":"31-OCT-2022","str_man_unit_name":"Micro Labs Limited"},{"str_drug_name":"Each Film Coated Tablet Contains: Brivaracetam 25 Mg/50 Mg/75 Mg/100 Mg","str_composition":"Brivaracetam 75.0000 Milligram (Mg)","str_indication":"As Adjunctive Therapy In The Treatment Of Partial -Onset Seizures In Patients 16 Years Of Age And Older With Epilepsy","dt_closure_dt":"22-MAR-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablet Contains: Brivaracetam 25 Mg/50 Mg/75 Mg/100 Mg","str_composition":"Brivaracetam 25.0000 Milligram (Mg)","str_indication":"As Adjunctive Therapy In The Treatment Of Partial -Onset Seizures In Patients 16 Years Of Age And Older With Epilepsy","dt_closure_dt":"22-MAR-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablet Contains: Brivaracetam 25 Mg/50 Mg/75 Mg/100 Mg","str_composition":"Brivaracetam 50.0000 Milligram (Mg)","str_indication":"As Adjunctive Therapy In The Treatment Of Partial -Onset Seizures In Patients 16 Years Of Age And Older With Epilepsy","dt_closure_dt":"22-MAR-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablet Contains: Brivaracetam 25 Mg/50 Mg/75 Mg/100 Mg","str_composition":"Brivaracetam 100.0000 Milligram (Mg)","str_indication":"As Adjunctive Therapy In The Treatment Of Partial -Onset Seizures In Patients 16 Years Of Age And Older With Epilepsy","dt_closure_dt":"22-MAR-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablet Contains: Cetilistat   120 Mg","str_composition":"Cetilistat 120.0000 Milligram (Mg)","str_indication":"Indicated For The Treatment Of Obesity (For Use Only In Patients Who Have Both Type 2 Diabetes Mellitus And Dyslipidemia And Whose Bmi Level Is 25kg/M2 Or More Even With Diet And Exercise Therapies)","dt_closure_dt":"21-SEP-2021","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Film Coated Tablet Contains: Imeglimin Hydrochloride 500 Mg/1000 Mg","str_composition":"Imeglimin Hydrochloride 1000.0000 Milligram (Mg)","str_indication":"In The Treatment Of Type Ii Diabetes","dt_closure_dt":"17-JAN-2023","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablet Contains: Imeglimin Hydrochloride 500 Mg/1000 Mg","str_composition":"Imeglimin Hydrochloride 500.0000 Milligram (Mg)","str_indication":"In The Treatment Of Type Ii Diabetes","dt_closure_dt":"17-JAN-2023","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablet Contains:- Lasmiditan Hemisuccinate 57.824 Mg/115.65 Mg/231.30 Mg Eq. To Lasmiditan?50mg/100mg/200mg","str_composition":"Lasmiditan Hemisuccinate Eq. To Lasmiditan 100.0000 Milligram (Mg)","str_indication":"Indicated For The Acute Treatment Of Migraine With Or Without Aura In Adult","dt_closure_dt":"29-NOV-2023","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Film Coated Tablet Contains:- Lasmiditan Hemisuccinate 57.824 Mg/115.65 Mg/231.30 Mg Eq. To Lasmiditan?50mg/100mg/200mg","str_composition":"Lasmiditan Hemisuccinate Eq. To Lasmiditan 50.0000 Milligram (Mg)","str_indication":"Indicated For The Acute Treatment Of Migraine With Or Without Aura In Adult","dt_closure_dt":"29-NOV-2023","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Film Coated Tablet Contains:- Lasmiditan Hemisuccinate 57.824 Mg/115.65 Mg/231.30 Mg Eq. To Lasmiditan?50mg/100mg/200mg","str_composition":"Lasmiditan Hemisuccinate Eq. To Lasmiditan 200.0000 Milligram (Mg)","str_indication":"Indicated For The Acute Treatment Of Migraine With Or Without Aura In Adult","dt_closure_dt":"29-NOV-2023","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Film Coated Tablets Contains: Efonidipine Hydrochloride Ethanolate 10 Mg/20 Mg/40 Mg","str_composition":"Efonidipine Hydrochloride Ethanolate 40.0000 Milligram (Mg)","str_indication":"Indicated For The Management Of ? Hypertension ? Renal Parenchymal Hypertension ? Angina","dt_closure_dt":"10-SEP-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablets Contains: Efonidipine Hydrochloride Ethanolate 10 Mg/20 Mg/40 Mg","str_composition":"Efonidipine Hydrochloride Ethanolate 20.0000 Milligram (Mg)","str_indication":"Indicated For The Management Of ? Hypertension ? Renal Parenchymal Hypertension ? Angina","dt_closure_dt":"10-SEP-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablets Contains: Efonidipine Hydrochloride Ethanolate 10 Mg/20 Mg/40 Mg","str_composition":"Efonidipine Hydrochloride Ethanolate 10.0000 Milligram (Mg)","str_indication":"Indicated For The Management Of ? Hypertension ? Renal Parenchymal Hypertension ? Angina","dt_closure_dt":"10-SEP-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablets Contains: Fimasartan Potassium Trihydrate Eq.To Fimasartan 30 Mg/60 Mg/120 Mg","str_composition":"Fimasartan Potassium Trihydrate Eq To Fimasartan 60.0000 Milligram (Mg)","str_indication":"For The Treatment Of Mild Hypertension","dt_closure_dt":"06-MAY-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablets Contains: Fimasartan Potassium Trihydrate Eq.To Fimasartan 30 Mg/60 Mg/120 Mg","str_composition":"Fimasartan Potassium Trihydrate Eq To Fimasartan 30.0000 Milligram (Mg)","str_indication":"For The Treatment Of Mild Hypertension","dt_closure_dt":"06-MAY-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablets Contains: Fimasartan Potassium Trihydrate Eq.To Fimasartan 30 Mg/60 Mg/120 Mg","str_composition":"Fimasartan Potassium Trihydrate Eq To Fimasartan 120.0000 Milligram (Mg)","str_indication":"For The Treatment Of Mild Hypertension","dt_closure_dt":"06-MAY-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablets Contains  Iguratimod 25 Mg","str_composition":"Iguratimod 25.0000 Milligram (Mg)","str_indication":"For The Treatment Of Active Rheumatoid Arthritis Symptoms","dt_closure_dt":"17-DEC-2019","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablets Contains:Obeticholic Acid  5mg/10mg","str_composition":"Obeticholic Acid 5.0000 Milligram (Mg)","str_indication":"It Is Indicated For The Treatment Of Primary Biliary Cholangitis (Also Known As Primary Biliary Cirrhosis) In Combination With Ursodeoxycholic Acid (Udca) In Adults With An Inadequate Response To Udca Or As Monotherapy In Adults Unable To Tolerate Udca.","dt_closure_dt":"21-APR-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Film Coated Tablets Contains:Obeticholic Acid  5mg/10mg","str_composition":"Obeticolic Acid 10.0000 Milligram (Mg)","str_indication":"It Is Indicated For The Treatment Of Primary Biliary Cholangitis (Also Known As Primary Biliary Cirrhosis) In Combination With Ursodeoxycholic Acid (Udca) In Adults With An Inadequate Response To Udca Or As Monotherapy In Adults Unable To Tolerate Udca.","dt_closure_dt":"21-APR-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Gastro Resistant Tablets Contains: Posaconazole 100 Mg","str_composition":"Posaconazole 100.0000 Milligram (Mg)","str_indication":"For Prophylaxis Of Invasive Aspregilus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus-Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia Form Chemotherapy.  Posaconazole Gastro Resistant Tablets Are Indicated In Patients 13 Years Of Age And Older","dt_closure_dt":"11-SEP-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each gm contains: Halobetasol 0.05% w/w + Mupirocin 2.0 % w/w gel","str_composition":"","str_indication":"For the topical treatment of inflammatory dermatitis withsecondry bacterial infection.","dt_closure_dt":"16.05.09","str_man_unit_name":""},{"str_drug_name":"Each Gram Contains: Naftifine Hydrochloride Usp 20 Mg  In Cream Base  Q.S","str_composition":"Naftifine Hydrochloride 2.0000 %W/W","str_indication":"Indicatede For The Treatment Of Superficial Fungal Infection Of The Skin (Tinea Corporis And Tinea Cruris)","dt_closure_dt":"26-MAY-2025","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Hard Gelatin Extended Release Capsule Contains Trimetazidine Hci Ip  80mg","str_composition":"Trimetazidine Hcl 80.0000 Milligram (Mg)","str_indication":"For The Treatment Of Ischaemic Heart Disease Angina Pectoris, Sequelae Of Infarction","dt_closure_dt":"07-DEC-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Ml Contains: Brivaracetam   10mg","str_composition":"Brivaracetam 10.0000 Mg/Ml","str_indication":"As Adjunctive Therapy In The Treatment Of Partial-Onset Seizures In Patients 16 Years Of Age And Older With Epilepsy","dt_closure_dt":"31-AUG-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each ml contains Calamine 15% w/v + Zinc oxide 5% w/v + Bentonite 3% w/v+Glycerin 5%w/v + Sodium citrate 0.05 % w/v lotion","str_composition":"","str_indication":"For the tretament of pruritis and prickly heat.","dt_closure_dt":"08.05.09","str_man_unit_name":""},{"str_drug_name":"Each Ml Contains: Clobazam Ip 2.5 Mg","str_composition":"Clobazam 2.5000 Mg/Ml","str_indication":"Indicated For Adjunctive Treatment Of Seizures Associated With Lennox-Gastaut Syndrome (Lgs) In Patients 2 Years Of Age Or Older","dt_closure_dt":"24-DEC-2020","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Ml Contains Ripasudil Hydrochloride Hydrate Eq To Ripasudil???4 Mg Benzalkonium Chloride Ip ??. 0.1mg","str_composition":"Ripasudil Hydrochloride Hydrate Eq. To Ripasudil 4.0000 Mg/Ml","str_indication":"To Treat Glaucoma And Ocular Hypertension When Other Medicines For Glaucoma Have Insufficient Effect Or Cannot Be Used","dt_closure_dt":"21-JAN-2022","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each sustained release tablet contains: Thiocolchicoside IP 8/16mg + Lornoxicam 8/16mg (Additional Strength)","str_composition":"","str_indication":"For the treatment of patients with acute painful musculoskeletal conditions.","dt_closure_dt":"08.04.13","str_man_unit_name":""},{"str_drug_name":"Each Uncoated Extended Release (Grs) Tablet Contains:- Baclofen Ip ??????.. 10mg","str_composition":"Baclofen 10.0000 Milligram (Mg)","str_indication":"For The Symptomatic Treatment Of Neuronal Spasticity Due To Multiple Sclerosis, Spinal Chord, Pathology & Injury","dt_closure_dt":"20-OCT-2021","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Uncoated Extended Release Tablets Contains: Baclofen Ip 20mg/30mg","str_composition":"Baclofen 30.0000 Milligram (Mg)","str_indication":"For The Symptomatic Treatment Of Neuronal Spasticity Due To Multiple Sclerosis, Spinal Chord, Pathology & Injury.","dt_closure_dt":"05-AUG-2020","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Uncoated Extended Release Tablets Contains: Baclofen Ip 20mg/30mg","str_composition":"Baclofen 20.0000 Milligram (Mg)","str_indication":"For The Symptomatic Treatment Of Neuronal Spasticity Due To Multiple Sclerosis, Spinal Chord, Pathology & Injury.","dt_closure_dt":"05-AUG-2020","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Uncoated Orodispersible Tablet Contains Bilastine 10mg","str_composition":"Bilastine 10.0000 Milligram (Mg)","str_indication":"For Symptomatic Treatment Of Allergic Rhino Conjunctivitis (Seasonal And Perennial) And Urticaria. It Is Indicated In Children Aged 6 To 11 Years With A Body Weight Of At Least 20kg","dt_closure_dt":"25-JUN-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Uncoated Sustained Release Tablet Contains Medroxyprogesterone Acetate Ip?.30mg","str_composition":"Medroxyprogesterone Acetate 30.0000 Milligram (Mg)","str_indication":"For The Treatment Of Endometriosis In Women","dt_closure_dt":"02-FEB-2022","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Un-Coated Tablet Contains: Ivermectin Ip 12 Mg","str_composition":"Ivermectin 12.0000 Milligram (Mg)","str_indication":"For The Treatment Of Patients With Mild To Moderate Covid-19 Disease","dt_closure_dt":"21-JAN-2022","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Uncoated Tablets Contain Lobeglitazone Sulfate   0.5 Mg","str_composition":"Lobeglitazone Sulfate 0.5000 Milligram (Mg)","str_indication":"Indicated For Treatment Of Adult Type 2 Diabetes Mellitus Patients: ?\tAs Monotherapy ?\tWho Are Inadequately Controlled By Diet And Exercise For Whom Metformin Is Inappropriate Because Of Contraindications Or Intolerance  ?\tAs Dual Oral Therapy In Combination With ?\tWho Are Inadequately Controlled By Diet And Exercise For Whom Metformin Despite Maximal Tolerated Dose Of Metformin Monotherapy.  ?\tWho Are Inadequately Controlled By Diet And Exercise And Taking A Sulphonyl Urea At Maximal Tolerated Dose Of Sulphonyl Urea Monotherapy In Which Metformin Is Inappropriate Because Of Contraindications Or Intolerance","dt_closure_dt":"19-JAN-2023","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Uncoated Tablets Contains Azilsartan Kamedoxomil Eq. To Azilsartan Medoxomil  20 Mg","str_composition":"Azilsartan Kamedoxomil Eq. To Azilsartan Medoxomil 20.0000 Milligram (Mg)","str_indication":"Indicated For The Treatment Of Hypertension In Adult Patients Either Alone Or In Combination With Other Antihypertensive Agents","dt_closure_dt":"11-MAY-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Uncoated Tablets Contains: Bilastine 20 Mg","str_composition":"Bilastine 20.0000 Milligram (Mg)","str_indication":"For Symptomatic Treatment Of Allergic Rhino-Conjuctivitis (Seasonal And Perennial) And Utricaria In Adults","dt_closure_dt":"04-MAR-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Uncoated Tablets Contains: Clobazam Ip 2.5 Mg & 7.5 Mg","str_composition":"Clobazam 7.5000 Milligram (Mg)","str_indication":"As An Adjunctive Therapy In Patients With Refractory Epilepsy.","dt_closure_dt":"09-NOV-2020","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Uncoated Tablets Contains: Clobazam Ip 2.5 Mg & 7.5 Mg","str_composition":"Clobazam 2.5000 Milligram (Mg)","str_indication":"As An Adjunctive Therapy In Patients With Refractory Epilepsy.","dt_closure_dt":"09-NOV-2020","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. Ltd."},{"str_drug_name":"Each Vial Contains Meropenem Trihydrate Equivalent To Anhydrous Meropenem Ip ?...2000mg Sodium Carbonate  Equivalent To Sodium (Na+) 180.4mg","str_composition":"Meropenem Trihydrate Equivalent To Anhydrous Meropenem 2000.0000 Milligram (Mg)","str_indication":"Nosocomial Pneumonia Like Hospital Acquired Pneumonia (Hap)/Ventilator Associated Pneumonia  ? Urinary Tract Infections Like Complicated Urinary Tract Infections  ? Intra-Abdominal Infection Like Complicated Intra-Abdominal Infection  ? Meningitis Like Acute Meningitis  ? Septicemia  ? Empiric Treatment Of Presumed Infection In Adult Patients With Febrile Neutropenia","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Each Vial Contains  Polymyxin B Sulphate Usp  Eq. To Polymyxin B ----- 500000 Iu (Sterile & Lyophilized )","str_composition":"Polymyxin B Sulphate  Eq. To Polymyxin B 500000.0000 Iu","str_indication":"Polymyxin B Sulfate Is A Drug Of Choice In The Treatment Of Infections Of The Urinary Tract, Meninges, And Blood Stream, Caused By Susceptible Strains Of Ps. Aeruginosa. It May Also Be Used As Subconjuctival Infection In The Treatment Of Infections Of The Eye Caused By Susceptible Strains Of Ps. Aeruginosa. It May Be Indicated In Serious Infections Caused By Susceptible Strains Of The Following Organisms, 1. H. Influenzae, Specifically Meningeal Infections 2. Escherichia Coli, Specifically Urinary Tract Infections 3. Aerobacter Aerogenes, Specifically Bacteremia 4. Klebsiella Pneumoniae, Specifically Bacteremia","dt_closure_dt":"30-DEC-2021","str_man_unit_name":"PURE & CURE HEALTHCARE Pvt. 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For The Treatment Of Deep Vein Thrombosis (Dvt) And Pulmonary Embolism (Pe), And For The Prevention Of Recurrent Dvt And Pe In Adults.","dt_closure_dt":"20-FEB-2025","str_man_unit_name":"Zuventus Healthcare Limited"},{"str_drug_name":"Edoxaban Tosylate Monohydrate","str_composition":"Edoxaban 0.0000 Not Applicable (Na)","str_indication":"NA","dt_closure_dt":"11-FEB-2025","str_man_unit_name":"Emcure Pharmaceuticals Limited"},{"str_drug_name":"Edoxaban Tosylate Monohydrate","str_composition":"Edoxaban 30.0000 Milligram (Mg)","str_indication":"In Prevention Of Stroke And Systemic Embolism In Adult Patients With Nonvalvular Atrial Fibrillation (Nvaf) With One Or More Risk Factors, Such As Congestive Heart Failure, Hypertension, Age ? 75 Years, Diabetes Mellitus, Prior Stroke Or Transient Ischaemic Attack (Tia).  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(This Treatment Should Only Be Used When Other Methods Of Supplementation, Particularly Iodization Of Salt And/Or Drinking Water, Cannot Be Undertaken) Hysterosalpingography (Hsg) In Adults","dt_closure_dt":"21-MAR-2025","str_man_unit_name":"Biophore India Pharmaceuticals Pvt Ltd"},{"str_drug_name":"Ethionamide","str_composition":"0.25-1 g","str_indication":"Anti-Tuberculosis drug, in cases resistant to other drugs.","dt_closure_dt":"1962- February","str_man_unit_name":"May & Bakers, Bombay"},{"str_drug_name":"Ethosuximide","str_composition":"TAB-250MG, Syrup-5ml=0.25g","str_indication":"Anticonvulsant for petitmal epilepsy","dt_closure_dt":"1961- December","str_man_unit_name":"Parke, Davis"},{"str_drug_name":"Ethyl esters of iodized fatty acids of poppy seed oil solution for injection 48%.","str_composition":"Each ampoule contains; ethyl esters of iodized fatty acids of poppy seed oil qs Iodine content; 48%, i.e. 480mg per ml","str_indication":"In  Diagnostic  Radiology: Lymphography  and Diagnosis  of  liver  lesions. 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"},{"str_drug_name":"Fimasartan Potassium Trihydrate","str_composition":"Fimasartan Potassium Trihydrate 120.0000 Milligram (Mg)","str_indication":"NA","dt_closure_dt":"15-OCT-2019","str_man_unit_name":"AMI LIFESCIENCES PRIVATE LIMITED"},{"str_drug_name":"Fimasartan Potassium Trihydrate","str_composition":"Fimasartan Potassium Trihydrate 100.0000 %","str_indication":"NA","dt_closure_dt":"15-FEB-2021","str_man_unit_name":"M/s Allastir Private Limited "},{"str_drug_name":"Fimasartan Potassium Trihydrate","str_composition":"Fimasartan Potassium Trihydrate 30.0000 Milligram (Mg)","str_indication":"NA","dt_closure_dt":"03-FEB-2020","str_man_unit_name":"HONOUR LAB LIMITED"},{"str_drug_name":"Fimasartan Potassium Trihydrate","str_composition":"Fimasartan Pottasium Trihydrate 100.0000 %","str_indication":"NA","dt_closure_dt":"09-JUL-2020","str_man_unit_name":"KIMIA BIOSCIENCES LIMITED"},{"str_drug_name":"Fimasartan Tablets  30/60/120mg","str_composition":"Fimasartan Tablets 60mg 60.0000 Milligram (Mg)","str_indication":"Fimasartan Is Indicated For The Treatment Of Mild To Moderate Essential Hypertension","dt_closure_dt":"16-APR-2020","str_man_unit_name":"Hetero Labs Limited"},{"str_drug_name":"Fimasartan Tablets  30/60/120mg","str_composition":"Fimasartan Tablets 30mg 30.0000 Milligram (Mg)","str_indication":"Fimasartan Is Indicated For The Treatment Of Mild To Moderate Essential Hypertension","dt_closure_dt":"16-APR-2020","str_man_unit_name":"Hetero Labs Limited"},{"str_drug_name":"Fimasartan Tablets  30/60/120mg","str_composition":"Fimasartan Tablets 120mg 120.0000 Milligram (Mg)","str_indication":"Fimasartan Is Indicated For The Treatment Of Mild To Moderate Essential Hypertension","dt_closure_dt":"16-APR-2020","str_man_unit_name":"Hetero Labs Limited"},{"str_drug_name":"Finasteride","str_composition":"1mg","str_indication":"Additional indication- in treatment of male pattern hair loss in men only.","dt_closure_dt":"23-04-2001","str_man_unit_name":"Cipla ltd."},{"str_drug_name":"Finasteride tabs","str_composition":"Each film coated tablet contains; finasteride-5mg","str_indication":"Benign prostatic hypertrophy only.","dt_closure_dt":"09/10/1996","str_man_unit_name":"Dr. Reddy lab"},{"str_drug_name":"Finerenone","str_composition":"Finerenone Micronized 20.0000 Milligram (Mg)","str_indication":"Finerenone Is Indicated To Reduce The Risk Of Cardiovascular Death, Hospitalization For Heart Failure, And Urgent Heart Failure Visits In Adult Patients With Heart Failure With Left Ventricular Ejection Fraction (Lvef) ? 40%","dt_closure_dt":"31-OCT-2025","str_man_unit_name":"Bayer Pharmaceuticals Pvt. 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","str_indication":"Indicated as a once daily maintenance bronchodilator treatment to relieve symptoms of patients with Chronic Obstructive Pulmonary Disease (COPD).","dt_closure_dt":"01.04.14","str_man_unit_name":""},{"str_drug_name":"Glycopyrronium Inhalation Solution 25mcg","str_composition":"Glycopyrrolate Ip Equivalent To Glycopyrronium 25.0000 Micrograms (?g)","str_indication":"Glycopyrronium Inhalation Solution Is Indicated For The Long-Term Maintenance Treatment Of Airflow Obstruction In Patients With Chronic Obstructive Pulmonary Disease (Copd), Including Chronic Bronchitis And/Or Emphysema","dt_closure_dt":"07-JUL-2021","str_man_unit_name":"Zydus Healthcare Limited"},{"str_drug_name":"Glycopyrronium Inhalation Solution 25 Mcg","str_composition":"Glycopyrrolate 100.0000 %","str_indication":"For The Long Term Maintenance Treatment Of Airflow Obstruction In Patients With Chronic Obstructive Pulmonary Disease (Copd) Including Chronic Bronchitis And/Or 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LTD."},{"str_drug_name":"Hepatitis-B Vaccine (recombinant)","str_composition":"20mcg/ml","str_indication":"","dt_closure_dt":"02/03/2000","str_man_unit_name":"Transgene vaccine ltd."},{"str_drug_name":"Hepatitis-B Vaccine (recombinant)","str_composition":"Each vial contains; Hepatitis B surface antigen (HBsAg)-20mcg/ml, 100mcg/100ml, 10mcg/0.5ml","str_indication":"For active immunization against Hepatitis-B","dt_closure_dt":"31-10-2000","str_man_unit_name":"V.H.Bhagat & Co."},{"str_drug_name":"Hepatitis B vaccine (recombinant DNA)","str_composition":"","str_indication":"For treatment of Hepatitis B virus infection.","dt_closure_dt":"1987-January","str_man_unit_name":"Eskayel, Bangalore"},{"str_drug_name":"Herpes Zoster Vaccine (Recombinant, Adjuvanted)","str_composition":"Ge 50.0000 Micrograms (?g),Sucrose 20.0000 Milligram (Mg),Polysorbate 80 (Ps80) 0.0800 Milligram (Mg),3-O-Desacyl-4?- Monophosphoryl Lipid A (Mpl) 50.0000 Milligram (Mg),Purified Quillaja Saponin (Qs-21) 50.0000 Micrograms (?g),Dioleoyl Phosphatidylcholine (Dopc) 1.0000 Milligram (Mg),Cholesterol 0.2500 Milligram (Mg),Sodium Chloride (Nacl) 4.3850 Milligram (Mg),Sodium Dihydrogen Phosphate Dihydrate (Nah2po4.2h20) 0.1600 Milligram (Mg),Dipotassium Phosphate (K2hpo4) 0.1160 Milligram (Mg),Disodium Phosphate Anhydrous (Na2hpo4) 0.1500 Milligram (Mg),Potassium Dihydrogen Phosphate (Kh2po4) 0.5400 Milligram (Mg),Water For Injection (Wfi) Q.S. 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Free) 20.0000 %","str_indication":"NA","dt_closure_dt":"29-MAY-2026","str_man_unit_name":"Biological E - Shameerpet"},{"str_drug_name":"Horse anti human lymphocyte globulin","str_composition":"","str_indication":"For aplastic anaemia.","dt_closure_dt":"1991- May","str_man_unit_name":"Alidac"},{"str_drug_name":"HPMC 0.3% +Dextran 0.1% + Glycerin 0.2%","str_composition":"","str_indication":"For the temporary relief of burning and irritation due to dryness of the eye and for use as a protection against further irritation. For the temporary relief of discomfort due to minorirritations of the eyes or to exposure to wind or sun.","dt_closure_dt":"06.07.10","str_man_unit_name":""},{"str_drug_name":"HSA free recombinant human erythropoietin injection","str_composition":"Each vial contains; HSA free recombinant erythropoietin injection-1000 IU, 2000 IU, 3000 IU, 4000 IU, 10000 IU","str_indication":"Additional strength.","dt_closure_dt":"07/12/2001","str_man_unit_name":"Wockhardt"},{"str_drug_name":"Human follicle stimulating Hormone (FSH) and Human leutenising harmone (LH)","str_composition":"","str_indication":"Fertility drug- to be supplied to gynaecologists attached to hospitals where facilities exist for screening patients and to private consultations of academic & professional standing.","dt_closure_dt":"1978-October","str_man_unit_name":"Searle, Bombay"},{"str_drug_name":"Human Insulin (Rdna Origin)","str_composition":"Human Insulin (Rdna Origin) 1.0000 Iu/0.0347 Mg","str_indication":"NA","dt_closure_dt":"11-MAY-2026","str_man_unit_name":"Regenix Drugs Ltd."},{"str_drug_name":"Human Insulin (r-DNA) Powder inhaler","str_composition":"","str_indication":"For type-I & Type-2 Diabetes.","dt_closure_dt":"30/08/2006","str_man_unit_name":""},{"str_drug_name":"Human interferon alfa-2b (reombinant) inj.","str_composition":"Each vial contains; human interferon alfa-2b (recombinant)-3mIU,5mIU,10mIU","str_indication":"By cancer specialists-for multiple myeloma, kaposis sarcoma in patients with AIDS, malignant melanoma, hairy cell leukemia, chronic myelogenous leukemia, laryngeal papilimatosis, condylomate accuminata, superficial and nodulocerative basal cell carcinoma.","dt_closure_dt":"02/01/2001","str_man_unit_name":"Kee pharma ltd, New Delhi"},{"str_drug_name":"Human Papillomavirus 9-Valent Vaccine, Recombinant [Serotypes: Type 6 L1, 11 L1, 16 L1, 18 L1, 31 L1, 33 L1, 45 L1, 52 L1 & 58 L1]","str_composition":"Human Papillomavirus Type 6 L1 Protein 30.0000 Micrograms (?g),Amorphous Aluminum Hydroxyphosphate Sulfate (As Adjuvant) 500.0000 Micrograms (?g),Human Papillomavirus Type 11 L1 Protein 40.0000 Micrograms (?g),Human Papillomavirus Type 16 L1 Protein 60.0000 Micrograms (?g),Human Papillomavirus Type 18 L1 Protein 40.0000 Micrograms (?g),Human Papillomavirus Type 31 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 33 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 45 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 52 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 58 L1 Protein 20.0000 Micrograms (?g),Sodium Chloride 9.5600 Milligram (Mg),L Histidine 0.7800 Milligram (Mg),Polysorbate 80 50.0000 Micrograms (?g),Sodium Borate 35.0000 Micrograms (?g)","str_indication":"Girls And Women (9-45 Years): Gardasil 9 Is A Vaccine Indicated In Girls And Women From 9 - 45 Years Of Age At 3 Dose Regimen (Schedule 0, 2 And 6 Months) For The Prevention Of Cervical, Vulvar, Vaginal, And Anal Cancer, Precancerous Or Dysplastic Lesions, Genital Warts, And Persistent Infections Caused By Human Papillomavirus (Hpv).,Boys And Men (9-45 Years): Gardasil 9 Is Indicated In Boys From 9 ? 45 Years Of Age At 3 Dose Regimen (Schedule: 0, 2 And 6 Months) For The Prevention Of External Genital Lesions And Persistent Infections And The Following Diseases Caused By Hpv Types Included In The Vaccine: ?\tAnal Cancer Caused By Hpv Types 16, 18, 31, 33, 45, 52, And 58. ?\tGenital Warts (Condyloma Acuminata) Caused By Hpv Types 6 And 11. And The Following Precancerous Or Dysplastic Lesions Caused By Hpv Types 6, 11, 16, 18, 31, 33, 45, 52, And 58: ?\tAnal Intraepithelial Neoplasia (Ain) Grades 1, 2, And 3.","dt_closure_dt":"18-FEB-2026","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Human Papillomavirus 9-Valent Vaccine, Recombinant [Serotypes: Type 6 L1, 11 L1, 16 L1, 18 L1, 31 L1, 33 L1, 45 L1, 52 L1 & 58 L1]","str_composition":"Human Papillomavirus Type 6 L1 Protein 30.0000 Micrograms (?g),Human Papillomavirus Type 45 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 16 L1 Protein 60.0000 Micrograms (?g),Human Papillomavirus Type 18 L1 Protein 40.0000 Micrograms (?g),L-Histidine 0.7800 Milligram (Mg),Human Papillomavirus Type 11 L1 Protein 40.0000 Micrograms (?g),Human Papillomavirus Type 33 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 52 L1 Protein 20.0000 Micrograms (?g),Sodium Chloride 9.5600 Milligram (Mg),Sodium Borate 35.0000 Micrograms (?g),Polysorbate 80 50.0000 Micrograms (?g),Human Papillomavirus Type 58 L1 Protein 20.0000 Micrograms (?g),Amorphous Aluminium Hydroxyphosphate Sulfate (As Adjuvant) 500.0000 Micrograms (?g),Human Papillomavirus Type 31 L1 Protein 20.0000 Micrograms (?g)","str_indication":"Human Papillomavirus 9-Valent Vaccine, Recombinant Is A Vaccine Indicated In Girls And Women From 9 Years To 26 Years At 03 Dose Regimen (Schedule: 0, 2 & 6 Months) For The Prevention Of Cervical, Vulvar, Vaginal And Anal Cancer;Precancerous Or Dysplastic Lesions, Genital Warts, And Persistent Infections Caused By Human Papillomavirus (Hpv).,Human Papillomavirus 9-Valent Vaccine, Recombinant Is A Vaccine Indicated In Boys From 9 Years To 15 Years At 03 Dose Regimen (Schedule: 0, 2 & 6 Months) For The Prevention Of External Genital Lesions And Persistent Infections And The Following Diseases Caused By Hpv Types Included In The Vaccine ? Anal Cancer Caused By Hpv Types 16, 18, 31, 33, 45, 52 And 58. ? Genital Warts (Condyloma Acuminate) Caused By Hpv Types 6 And 11. ? And The Following Precancerous Or Dysplastic Lesions Caused By Hpv Types 6, 11, 16, 18, 31, 33, 45, 52 And 58. ? Anal Intraepithelial Neoplasia (Ain) Grades 1, 2 And 3","dt_closure_dt":"10-DEC-2025","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Human Papillomavirus 9-Valent Vaccine, Recombinant [Serotypes: Type 6 L1, 11 L1, 16 L1, 18 L1, 31 L1, 33 L1, 45 L1, 52 L1 & 58 L1]","str_composition":"Human Papillomavirus Type 6 L1 Protein 30.0000 Micrograms (?g),Human Papillomavirus Type 11 L1 Protein 40.0000 Micrograms (?g),Human Papillomavirus Type 16 L1 Protein 60.0000 Micrograms (?g),Human Papillomavirus Type 18 L1 Protein 40.0000 Micrograms (?g),Human Papillomavirus Type 31 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 33 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 45 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 52 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 58 L1 Protein 20.0000 Micrograms (?g),Amorphous Aluminum Hydroxyphosphate Sulfate (As Adjuvant) 500.0000 Micrograms (?g),Sodium Chloride 9.5600 Milligram (Mg),L-Histidine 0.7800 Milligram (Mg),Polysorbate 80 50.0000 Micrograms (?g),Sodium Borate 35.0000 Micrograms (?g)","str_indication":"Girls And Women (9-45 Years): Gardasil 9 Is A Vaccine Indicated In Girls And Women From 9 - 45 Years Of Age At 3 Dose Regimen (Schedule 0, 2 And 6 Months) For The Prevention Of Cervical, Vulvar, Vaginal, And Anal Cancer, Precancerous Or Dysplastic Lesions, Genital Warts, And Persistent Infections Caused By Human Papillomavirus (Hpv).,Boys And Men (9-45 Years): Gardasil 9 Is Indicated In Boys From 9 ? 45 Years Of Age At 3 Dose Regimen (Schedule: 0, 2 And 6 Months) For The Prevention Of External Genital Lesions And Persistent Infections And The Following Diseases Caused By Hpv Types Included In The Vaccine: ?\tAnal Cancer Caused By Hpv Types 16, 18, 31, 33, 45, 52, And 58. ?\tGenital Warts (Condyloma Acuminata) Caused By Hpv Types 6 And 11. And The Following Precancerous Or Dysplastic Lesions Caused By Hpv Types 6, 11, 16, 18, 31, 33, 45, 52, And 58: ?\tAnal Intraepithelial Neoplasia (Ain) Grades 1, 2, And 3.","dt_closure_dt":"06-AUG-2025","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Human Papillomavirus Quadrivalent (Types 6, 11, 16, And 18) Vaccine, Recombinant","str_composition":"Virus Like Particles (Vlp) Of R-(L-1) Protein Of Hpv Type 6 20.0000 Micrograms (?g),Virus Like Particles (Vlp) Of R-(L-1) Protein Of Hpv Type 11 40.0000 Micrograms (?g),Virus Like Particles (Vlp) Of R-(L-1) Protein Of Hpv Type 16 40.0000 Micrograms (?g),Virus Like Particles (Vlp) Of R-(L-1) Protein Of Hpv Type 18 20.0000 Micrograms (?g),Amorphous Aluminum Hydroxy-Phosphate Sulfate (As Adjuvant) 225.0000 Micrograms (?g),Sodium Chloride 9.5600 Milligram (Mg),L-Histidine 0.7800 Milligram (Mg),Polysorbate 80 50.0000 Micrograms (?g),Sodium Borate 35.0000 Micrograms (?g)","str_indication":"Gardasil Is Indicated In Females Aged 9 Through 45 Years \"For Prevention Of Cervical, Vulvar, And Vaginal Cancer, Precancerous Or Dysplastic Lesions, Genital Warts (Condyloma Acuminata), And Infection Caused By Human Papillomavirus (Hpv) Types 6, 11, 16 And 18 (Which Are Included In The Vaccine).","dt_closure_dt":"24-FEB-2026","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Human Papillomavirus Vaccine Rdna Ph. Eur.","str_composition":"Hpv-16 L1 Vlp 20.0000 Micrograms (?g),Hpv-18 L1 Vlp 20.0000 Micrograms (?g),3-O-Desacyl-4? Monophoshoryl Lipid A (Mpl) 50.0000 Micrograms (?g),Aluminium (Hydroxide Salt) 500.0000 Micrograms (?g),Sodium Chloride (Nacl) 4.4000 Mg (150 Mm),Sodium Dihydrogen Phosphate Dihydrate (Nah2po4.2h2o) 0.6240 Mg (8 Mm),Water For Injection 0.5000 Ml (Q.S. Ad)","str_indication":"Cervarix Is Indicated In Females From 9 To 45 Years Of Age For The Prevention Of Cervical And Anal Premalignant Lesions And Cancers Causally Related To Certain Oncogenic Human Papillomavirus (Hpv) Types.","dt_closure_dt":"16-MAR-2020","str_man_unit_name":"GlaxoSmithKline Asia Private Limited"},{"str_drug_name":"Human placental Extract ","str_composition":"","str_indication":"","dt_closure_dt":"1978-September","str_man_unit_name":"Curewel (I)"},{"str_drug_name":"Human recombinant granulocyte colony stimulating factor (Hu r GCSF) inj.","str_composition":"Each ml contains; Hu r GCSF-300mcg","str_indication":"For decreasing the severity of cytotoxic chemotherapy induced neutropenia, acceleration.","dt_closure_dt":"28-06-2001","str_man_unit_name":"Dr. Reddy"},{"str_drug_name":"Hyaluronic acid (cross linked) Pre-filled syringe 18mg/0.6ml and 24mg/0.8ml","str_composition":"","str_indication":"For intradermal implantation and facial soft tissue augmentation.","dt_closure_dt":"31.01.09","str_man_unit_name":""},{"str_drug_name":"Hyaluronic acid injection","str_composition":"Each ml contains; 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This Vaccine Should Be Administered In Accordance With Official Recommendations.","dt_closure_dt":"11-JUN-2021","str_man_unit_name":"SANOFI HEALTHCARE INDIA PRIVATE LIMITED"},{"str_drug_name":"Inactivated Hepatitis A Vaccine Adsorbed I.P.","str_composition":"Hepatitis A Virus, Gbm Strain (Inactivated) 80.0000 U,Formaldehyde 12.5000 Micrograms (?g),Ethanol Anhydrous 2.5000 ?l,2-Phenoxyethanol 2.5000 ?l,Hanks Medium 199 0.0000 Q.S To 0.5 Ml,Aluminium Hydroxide 0.1500 Milligram (Mg),Sodium Hydroxide And Hydrochloric Acid 0.0000 Ph Adjuster","str_indication":"For Prevention Of Infections Caused By Hepatitis A Virus In Children In The Age Group Of 12 Months To 15 Years","dt_closure_dt":"03-JUN-2021","str_man_unit_name":"SANOFI HEALTHCARE INDIA PRIVATE LIMITED"},{"str_drug_name":"Inactivated Influenza Vaccine (Split Virion) Ip","str_composition":"A/Michigan/45/2015 (H1n1)Pdm09-Like Strain (A/Singapore/Gp1908/2015, Ivr-180) 15.0000 Micrograms Ha,A/Hong Kong/4801/2014(H3n2)-Like Strain (A/Hong Kong/4801/2014, Nymc X-263b) 15.0000 Micrograms Ha,B/Brisbane/60/2008-Like Strain (B/Brisbane/60/2008, Wild Type) [Victoria Lineage] 15.0000 Micrograms Ha,B/Phuket/3073/2013-Like Strain (B/Phuket/3073/2013, Wild Type) [Yamagata Lineage] 15.0000 Micrograms Ha,Polysorbate 80 (Tween-80) 550.0000 Micrograms (?g),Octoxinol 10 (Triton� X-100) 115.0000 Micrograms (?g),Rrr-?-Tocopheryl Hydrogen Succinate 135.0000 Micrograms (?g),Sodium Chloride 3.7500 Milligram (Mg),Magnesium Chloride Hexahydrate 0.0500 Milligram (Mg),Disodium Phosphate Dodecahydrate 1.3000 Milligram (Mg),Potassium Dihydrogen Phosphate 0.2000 Milligram (Mg),Potassium Chloride 0.1000 Milligram (Mg),Formaldehyde 0.0050 Milligram (Mg),Sodium Deoxycholate 0.0650 Milligram (Mg),Ovalbumin 0.0500 Micrograms (?g),Gentamicin Sulphate 0.0000 (Traces),Hydrocortisone 0.0000 Traces,Water For Injections 0.5000 Ml","str_indication":"Fluarix-Tetra Is Indicated For Active Immunization Of Adults And Children From 6 Months Of Age For The Prevention Of Influenza Disease Caused By The Two Influenza A Virus Subtypes And The Two Influenza B Virus Types Contained In The Vaccine.","dt_closure_dt":"24-MAR-2020","str_man_unit_name":"GLAXOSMITHKLINE PHARMACEUTICALS LIMITED"},{"str_drug_name":"Inactivated Influenza Vaccine (Split Virion) Ip","str_composition":"A/Victoria/2570/2019 (H1n1)Pdm09-Like Strain(A/Victoria/2570/2019 (H1n1) Ivr-215) 15.0000 Micrograms (?g),A/Hong Kong/2671/2019 (H3n2)-Like Strain(A/Hong Kong/2671/2019 (H3n2) Nib-121) 15.0000 Micrograms (?g),B/Washington/02/2019-Like Strain (B/Washington/02/2019, Wild Type) [Victoria Lineage] 15.0000 Micrograms (?g),B/Phuket/3073/2013-Like Strain(B/Phuket/3073/2013, Wild Type) [Yamagata Lineage] 15.0000 Micrograms (?g),Polysorbate 80 (Tween-80) 550.0000 Micrograms (?g),Octoxinol 10 (Triton� X-100) 115.0000 Micrograms (?g),Rrr-?-Tocopheryl Hydrogen Succinate 135.0000 Micrograms (?g),Sodium Chloride 3.8000 Milligram (Mg),Magnesium Chloride Hexahydrate 0.0500 Milligram (Mg),Disodium Phosphate Dodecahydrate 1.3000 Milligram (Mg),Potassium Dihydrogen Phosphate 0.2000 Milligram (Mg),Potassium Chloride 0.1000 Milligram (Mg),Water For Injections Ad 0.5000 Ml,Formaldehyde 0.0050 Milligram (Mg),Sodium Deoxycholate 0.0650 Milligram (Mg),Ovalbumin 0.0500 Micrograms (?g),Gentamicin Sulphate 0.0000 Traces,Hydrocortisone 0.0000 Traces","str_indication":"Fluarix-Tetra Is Indicated For Active Immunisation Of Adults And Children From 6 Months Of Age For The Prevention Of Influenza Disease Caused By The Two Influenza A Virus Subtypes And The Two Influenza B Virus Lineages Contained In The Vaccine","dt_closure_dt":"09-MAY-2022","str_man_unit_name":"GLAXOSMITHKLINE PHARMACEUTICALS LIMITED"},{"str_drug_name":"Inactivated Influenza Vaccine (Split Virion) I.P","str_composition":"A/H3n2 15.0000 Micrograms Haemagglutinin Per Strain Plus Overage,A/H1n1 15.0000 Micrograms Haemagglutinin Per Strain Plus Overage,B 15.0000 Micrograms Haemagglutinin Per Strain Plus Overage,Phosphate Buffered Saline Solution (Potassium Dihydrogen Phosphate) 0.2000 Gram (G),Phosphate Buffered Saline Solution (Disodium Phosphate Dihydrate) 1.1500 Gram (G),Phosphate Buffered Saline Solution (Potassium Chloride) 0.2000 Gram (G),Phosphate Buffered Saline Solution (Sodium Chloride) 8.0000 Gram (G),Phosphate Buffered Saline Solution (Water For Injections) 0.0000 Up To 1000 Ml,Thiomersal 2.0000 Micrograms (?g)","str_indication":"Prophylaxis Of Influenza.","dt_closure_dt":"25-OCT-2021","str_man_unit_name":"SANOFI HEALTHCARE INDIA PRIVATE LIMITED"},{"str_drug_name":"Inactivated Influenza Vaccine (Split Virion) I.P.","str_composition":"A/Michigan/45/2015 (H1n1) Pdm09 - Like Strain (A/Singapore/Gp1908/2015, Ivr-180) 15.0000 Microgram Ha,A/Hong Kong/4801/2014 (H3n2) - Like Strain (A/Hong Kong/4801/2014, Nymc X-263b) 15.0000 Microgram Ha,B/Brisbane/60/2008 ? Like Strain (B/Brisbane/60/2008, Wild Type) [Victoria Lineage] 15.0000 Microgram Ha,B/Phuket/3073/2013 ? Like Strain (B/Phuket/3073/2013, Wild Type) [Yamagata Lineage] 15.0000 Microgram Ha,Polysorbate 80 (Tween-80) 550.0000 Micrograms (?g),Octoxinol 10 (Triton� X-100) 115.0000 Micrograms (?g),Rrr-Alpha-Tocopheryl Hydrogen Succinate 135.0000 Micrograms (?g),Sodium Chloride 3.7500 Milligram (Mg),Magnesium Chloride Hexahydrate 0.0500 Milligram (Mg),Disodium Phosphate Dodecahydrate 1.3000 Milligram (Mg),Potassium Dihydrogen Phosphate 0.2000 Milligram (Mg),Potassium Chloride 0.1000 Milligram (Mg),Water For Injection 0.5000 Ml (Qs),Formaldehyde 0.0050 Milligram (Mg),Sodium Deoxycholate 0.0650 Milligram (Mg),Ovalbumin 0.0500 Micrograms (?g),Gentamicin Sulphate 0.0000 (Traces),Hydrocortisone 0.0000 (Traces)","str_indication":"Fluarix-Tetra Is Indicated For Active Immunisation Of Adults And Children From 6 Months Of Age For The Prevention Of Influenza Disease Caused By The Two Influenza A Virus Subtypes And The Two Influenza B Virus Types Contained In The Vaccine.","dt_closure_dt":"04-APR-2019","str_man_unit_name":"GLAXOSMITHKLINE PHARMACEUTICALS LIMITED"},{"str_drug_name":"Inactivated Influenza Vaccine (Split Virion) I.P.","str_composition":"Disodium Hydrogen Phosphate Dodecahydrate 1.3000 Milligram (Mg),Ovalbumin 0.0500 Micrograms (?g),Octoxinol 10 (Triton� X-100) 85.0000 Micrograms (?g),Sodium Chloride 3.8000 Milligram (Mg),Formaldehyde 5.0000 Micrograms (?g),Magnesium Chloride Hexahydrate 0.0500 Milligram (Mg),A/Victoria/4897/2022 (H1n1) Pdm09-Like Strain (A/Victoria/4897/2022, Ivr-238) 15.0000 Microgram Haemagglutinin,A/Thailand/8/2022 (H3n2)-Like Strain (A/Thailand/8/2022, Ivr-237) 15.0000 Microgram Haemagglutinin,Polysorbate 80 (Tween-80) 415.0000 Micrograms (?g),Hydrocortisone 0.0015 Micrograms (?g),Potassium Chloride 0.1000 Milligram (Mg),Gentamicin Sulphate 0.1500 Micrograms (?g),Water For Injections 0.5000 Ml (Qs),Sodium Deoxycholate 50.0000 Micrograms (?g),Potassium Dihydrogen Phosphate 0.1900 Milligram (Mg),B/Austria/1359417/2021-Like Strain (B/Austria/1359417/2021, Bvr-26) 15.0000 Microgram Haemagglutinin,Rrr-?-Tocopheryl Hydrogen Succinate 100.0000 Micrograms (?g)","str_indication":"Fluarix Is Indicated For Active Immunisation Of Adults And Children From 6 Months Of Age For The Prevention Of Influenza Disease Caused By The Two Influenza A Virus Subtypes And One Influenza B Virus Lineage Contained In The Vaccine","dt_closure_dt":"17-SEP-2025","str_man_unit_name":"GLAXOSMITHKLINE PHARMACEUTICALS LIMITED"},{"str_drug_name":"Inactivated Influenza Vaccine (Split Virion) I.P. (Tetravalent)","str_composition":"A/Michigan/45/2015 (H1n1) Like Virus 7.5000 Micrograms (?g),A/Hong Kong/4801/2014 (H3n2) Like Virus 7.5000 Micrograms (?g),B/Phuket/3073/2013 Like Virus 7.5000 Micrograms (?g),B/Brisbane/60/2008 Like Virus 7.5000 Micrograms (?g)","str_indication":"It Is Indicated For Active Immunization Of Adults And Children From 6 Months Of Age And Older For The Prevention Of Influenza Disease Caused By The Two Influenza A Virus Subtypes And The Two Influenza B Virus Types Contained In The Vaccine.","dt_closure_dt":"12-JUN-2019","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Inactivated Influenza Vaccine (Split Virion) I.P. (Tetravalent)","str_composition":"A/Michigan/45/2015 (H1n1) Like Virus 15.0000 Micrograms (?g),A/Hong Kong/4801/2014 (H3n2) Like Virus 15.0000 Micrograms (?g),B/Phuket/3073/2013 Like Virus 15.0000 Micrograms (?g),B/Brisbane/60/2008 Like Virus 15.0000 Micrograms (?g)","str_indication":"It Is Indicated For Active Immunization Of Adults And Children From 6 Months Of Age And Older For The Prevention Of Influenza Disease Caused By The Two Influenza A Virus Subtypes And The Two Influenza B Virus Types Contained In The Vaccine.","dt_closure_dt":"12-JUN-2019","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Inactivated Influenza Vaccine (Split Virion) I.P. (Tetravalent) ? 0.5 Ml","str_composition":"A/Sydney/5/2021 (H1n1) Pdm09 ? Like Virus 15.0000 ?g Ha,A/Darwin/9/2021 (H3n2) ? Like Virus 15.0000 ?g Ha,B/Austria/1359417/2021 (B/Victoria Lineage) ? Like Virus 15.0000 ?g Ha,B/Phuket/3073/2013 (B/Yamagata Lineage) ? Like Virus 15.0000 ?g Ha","str_indication":"Vaxiflu-4 Is Indicated In Children From 6 Months To 17 Years And Adults ? 18 Years Of Age For Active Immunization For The Prevention Of Disease Caused By Influenza A Subtype Viruses And Type B Viruses Contained In The Vaccine.","dt_closure_dt":"24-MAY-2023","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Inactivated Influenza Vaccine (Split Virion) I.P. (Trivalent)","str_composition":"A/Victoria/4897/2022 (H1n1) Pdm09 ? Like Virus 15.0000 ?g Ha,A/Thailand/8/2022 (H3n2) ? Like Virus 15.0000 ?g Ha,B/Austria/1359417/2021 (B/Victoria Lineage) ? Like Virus 15.0000 ?g Ha","str_indication":"It Is Indicated In Children From 6 Months To 17 Years And Adults ? 18 Years Of Age For Active Immunization For The Prevention Of Disease Caused By Influenza A Subtype Viruses And Type B Viruses Contained In The Vaccine.","dt_closure_dt":"24-APR-2025","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Inactivated Influenza Vaccine (Surface Antigen)","str_composition":"An A/Michigan/45/2015 (H1n1) 15.0000 ?g/Ml,An A/Hong Kong/4801/2014 (H3n2) 15.0000 ?g/Ml,A B/Brisbane/60/2008- 15.0000 ?g/Ml,B/Phuket/3073/2013 15.0000 ?g/Ml","str_indication":"Prophylaxis Of Influenza, Especially Those Who Run An Increased Risk Of Associated Complications","dt_closure_dt":"16-JUL-2019","str_man_unit_name":"Abbott India Limited"},{"str_drug_name":"Inactivated Influenza Vaccine (Surface Antigen) I.P. (Quadrivalent)","str_composition":"A/Michigan/45/2015 (H1n1)Pdm09-Like Strain (A/Singapore/Gp1908/2015, Ivr- 180) 15.0000 ?g/Ml,A/Singapore/Infimh-16-0019/2016 (H3n2)-Like Strain (A/Singapore/Infimh- 16-0019/2016, Nib-104) 15.0000 ?g/Ml,B/Phuket/3073/2013-Like Strain (B/Phuket/3073/2013, Wild Type) 15.0000 ?g/Ml,B/Brisbane/60/2008-Like Strain (B/Brisbane/60/2008, Wild Type) 15.0000 ?g/Ml","str_indication":"Prophylaxis Of Influenza, Especially Those Who Run An Increased Risk Of Associated Complications. Inactivated Influenza Vaccine (Surface Antigen) I.P. (Quadrivalent) Is Indicated In Adults And Children From 6 Months Of Age","dt_closure_dt":"14-FEB-2020","str_man_unit_name":"Abbott India Limited"},{"str_drug_name":"Inactivated Poliomyelitis Monovalent Bulk Type 1, Inactivated Poliomyelitis Monovalent Bulk Type 2 And Inactivated Poliomyelitis Monovalent Bulk Type 3","str_composition":"Inactivated Poliomyelitis Virus Type 1, Mahoney Strain 1250.0000 Du/Ml,Inactivated Poliomyelitis Virus Type 2, Mef -1 Strain 430.0000 Du/Ml,Inactivated Poliomyelitis Virus Type 3, Saukett Strain 520.0000 Du/Ml","str_indication":"NA","dt_closure_dt":"17-MAR-2026","str_man_unit_name":"SERUM INSTITUTE OF INDIA PVT. LTD."},{"str_drug_name":"Inactivated purified rabies vaccine (pitman moore strain propagated on duck embryo)","str_composition":"Each vial contains; inactivated purified rabies virus (pitman moore strain propagated in duck embryo)-�?� 2.5 IU","str_indication":"Active immunization against rabies.","dt_closure_dt":"12/07/2002","str_man_unit_name":"Cadila healthcare ltd."},{"str_drug_name":"Inactivated Rabies Vaccine (Human diploid cell)","str_composition":"","str_indication":"Antirabies- For the treatment of rabies.","dt_closure_dt":"1981-April","str_man_unit_name":"Bnagal Traders, Bombay"},{"str_drug_name":"Inactivated Rabies Virus (Flury Lep) Vaccine Drug Substance","str_composition":"Inactivated Rabies Virus (Flury Lep) 40.0000 Iu/Ml","str_indication":"NA","dt_closure_dt":"08-APR-2025","str_man_unit_name":"CHIRON BEHRING VACCINES PVT. LTD."},{"str_drug_name":"Inactivated Salk Polio Vaccine (Adsorbed)","str_composition":"Inactivated Poliomyelitis Virus Type 1, Mahoney Strain 10.0000 D Antigen Units,Inactivated Poliomyelitis Virus Type 2, Mef -1 Strain 2.0000 D Antigen Units,Inactivated Poliomyelitis Virus Type 3, Saukett Strain 10.0000 D Antigen Units,Aluminium Hydroxide Al (Oh)3 1.2500 Milligram (Mg),2-Phenoxyethanol 2.5000 Milligram (Mg),Formaldehyde 12.5000 Micrograms (?g)","str_indication":"For Active Immunization Of Infants (As Young As 6 Weeks Of Age), Children And Adults For Prevention Of Poliomyelitis Caused By Poliovirus Types 1, 2, And 3","dt_closure_dt":"24-FEB-2026","str_man_unit_name":"SERUM INSTITUTE OF INDIA PVT. LTD."},{"str_drug_name":"Inactivate Hepatitis A Vaccine (Adsorbed) I.P.","str_composition":"Inactivated Hav Antigen (Tz84 Strain) 250.0000 U,Aluminum (As Aluminum Hydroxide) 0.1750 Milligram (Mg),Disodium Hydrogen Phosphate 0.5000 Ml Q.S,Sodium Chloride 4.2500 Milligram (Mg),Sodium Dihydrogen Phosphate 0.5000 Ml Q.S,Water For Injection 0.5000 Ml Q.S","str_indication":"Active Immunization Against Infection Caused By Hepatitis A Virus","dt_closure_dt":"13-APR-2021","str_man_unit_name":"Biological E - Shameerpet"},{"str_drug_name":"Inclisiran Solution For Injection In Prefilled Syringe 284 Mg/1.5 Ml","str_composition":"Inclisiran (Equivalent To 300 Mg Inclisiran Sodium) 284.0000 Milligram (Mg)","str_indication":"Inclisiran Is Indicated In Adults With Primary Hypercholesterolaemia (Heterozygous Familial And Non Familial) Or Mixed Dyslipidaemia, As An Adjunct To Diet: ?\tIn Combination With A Statin Or Statin With Other Lipid Lowering Therapies In Patients Unable To Reach Ldl C Goals With The Maximum Tolerated Dose Of A Statin, Or ?\tAlone Or In Combination With Other Lipid Lowering Therapies In Patients Who Are Statin Intolerant, Or For Whom A Statin Is Contraindicated.","dt_closure_dt":"22-SEP-2023","str_man_unit_name":"Novartis Healthcare Private Limited"},{"str_drug_name":"Indacaterol Acetate","str_composition":"Indacaterol Acetate 98.0000 %","str_indication":"NA","dt_closure_dt":"21-OCT-2024","str_man_unit_name":"Cipla Limited"},{"str_drug_name":"Indacaterol Acetate","str_composition":"Indacaterol Acetate 100.0000 %","str_indication":"NA","dt_closure_dt":"18-MAY-2022","str_man_unit_name":"MELODY HEALTHCARE PVT.LTD"},{"str_drug_name":"Indacaterol (as Maleate) capsules 150mcg/300mcg","str_composition":"Each capsule contains; indacaterol 150mcg, 300mcg (as Indacaterol Maleate)","str_indication":"For maintenance bronchodilator treatment of airflow obstruction in adult patients with chronic obstructive pulmonary disease (COPD).","dt_closure_dt":"28.02.2014","str_man_unit_name":"Cipla ltd."},{"str_drug_name":"Indacaterol (as Maleate) Inhalation Powder Hard Capsules �?�.. ...150/300mcg","str_composition":"Each capsule contains; indacaterol maleate eq.to indacaterol-150mcg, 300mcg","str_indication":"For maintenance bronchodilator treatment of airflow obstruction in adult patients with chronic obstructive pulmonary disease (COPD).","dt_closure_dt":"28.04.10","str_man_unit_name":"Novartis healthcare, Mumbai"},{"str_drug_name":"Indacaterol+Mometasone Furoate","str_composition":"Indacaterol Acetate 150.0000 Mcg,Mometasone Furoate 80.0000 Mcg","str_indication":"Indacaterol + Mometasone Furoate Powder For Inhalation Is Indicated As A Maintenance Treatment Of Asthma In Adults And Adolescents 12 Years Of Age And Older Not Adequately Controlled With Inhaled Corticosteroids And Inhaled Short-Acting Beta2-Agonists.","dt_closure_dt":"24-MAY-2022","str_man_unit_name":"Glenmark Pharmaceuticals Ltd."},{"str_drug_name":"Indacaterol+Mometasone Furoate","str_composition":"Indacaterol Acetate 150.0000 Mcg,Mometasone Furoate 160.0000 Mcg","str_indication":"Indacaterol + Mometasone Furoate Powder For Inhalation Is Indicated As A Maintenance Treatment Of Asthma In Adults And Adolescents 12 Years Of Age And Older Not Adequately Controlled With Inhaled Corticosteroids And Inhaled Short-Acting Beta2-Agonists.","dt_closure_dt":"24-MAY-2022","str_man_unit_name":"Glenmark Pharmaceuticals Ltd."},{"str_drug_name":"Indacaterol+Mometasone Furoate","str_composition":"Indacaterol Acetate 150.0000 Mcg,Mometasone Furoate 320.0000 Mcg","str_indication":"Indacaterol + Mometasone Furoate Powder For Inhalation Is Indicated As A Maintenance Treatment Of Asthma In Adults And Adolescents 12 Years Of Age And Older Not Adequately Controlled With Inhaled Corticosteroids And Inhaled Short-Acting Beta2-Agonists.","dt_closure_dt":"24-MAY-2022","str_man_unit_name":"Glenmark Pharmaceuticals Ltd."},{"str_drug_name":"Indapamide Hemihydrate ","str_composition":"Each tablet contains; 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Indomethacin-50mg, 100mg","str_indication":"","dt_closure_dt":"1970- July","str_man_unit_name":"Merck, Sharp & Dohme"},{"str_drug_name":"Infectious bursal disease vaccine inactivated","str_composition":"","str_indication":"Bursal disease vaccine- In the treatment of infectious bursal disease in poultry.","dt_closure_dt":"1986-March","str_man_unit_name":"Ventri biological, Pune"},{"str_drug_name":"Infectious coryza vaccine (Inactivated)","str_composition":"","str_indication":"","dt_closure_dt":"1987-March","str_man_unit_name":"Venkaterwara"},{"str_drug_name":"Infliximab 100 Mg","str_composition":"Infliximab 100.0000 Milligram (Mg),Sodium Hydrogen Phosphate Dihydrate 6.1000 Milligram (Mg),Sodium Dihydrogen Phosphate Dihydrate 2.2000 Milligram (Mg),Polysorbate 80 0.5000 Milligram (Mg),Sucrose 500.0000 Milligram (Mg)","str_indication":"Rheumatoid Arthritis,Psoriatic Arthritis,Ankylosing Spondylitis (Bechterew?S Disease),Psoriasis,Crohn?S Disease,Ulcerative Colitis","dt_closure_dt":"01-JAN-2020","str_man_unit_name":"BIOCAD INDIA PVT LTD,"},{"str_drug_name":"Infliximab inj.","str_composition":"Each vial contains; infliximab 100mg in 10ml ","str_indication":"Reduction of signs & symptoms of rheumatoid arthritis in patients who have an inadequate response to methotrexate (additional indication).","dt_closure_dt":"04/10/2001","str_man_unit_name":"Fulford India ltd."},{"str_drug_name":"Infliximab injection","str_composition":"","str_indication":"For additional indication- in maintenance therapy of Crohn's disease & fistulising Crohn's disease.","dt_closure_dt":"15/07/2004","str_man_unit_name":"Fulford ltd."},{"str_drug_name":"Infliximab injection","str_composition":"","str_indication":"For additional indication of- maintenance therapy in crohn's disease, fistulising crohn's diase and maintenance therapy in fistulizing crohn's disease.","dt_closure_dt":"01/09/2004","str_man_unit_name":"Fulford ltd."},{"str_drug_name":"Infliximab i.v injection","str_composition":"Each 10ml vial contains infliximab-100mg","str_indication":"For treatment of moderate to severly active crohn's disease for the reduction of signs and symptoms in patients who have an inadequate response to conventional therapies.","dt_closure_dt":"25-01-2000","str_man_unit_name":"Fulford India Ltd."},{"str_drug_name":"Infliximab Powder For Concentrate For Solution For Infusion","str_composition":"Infliximab (Pf-06438179) 100.0000 Milligram (Mg),Polysorbate 80 0.5000 Milligram (Mg),Sucrose 250.0000 Milligram (Mg),Disodium Succinate Hexahydrate 12.1000 Milligram (Mg),Succinic Acid 0.6000 Milligram (Mg)","str_indication":"Infliximab Is Indicated For Reducing Signs And Symptoms And Inducing And Maintaining Clinical Remission In Adult Patients With Moderately To Severely Active Crohn?S Disease Who Have Had An Inadequate Response To Conventional Therapy.,Infliximab Is Indicated For Reducing The Number Of Draining Enterocutaneous And Rectovaginal Fistulas And Maintaining Fistula Closure In Adult Patients With Fistulizing Crohn?S Disease.,Infliximab Is Indicated For Reducing Signs And Symptoms And Inducing And Maintaining Clinical Remission In Pediatric Patients 6 Years Of Age And Older With Moderately To Severely Active Crohn?S Disease Who Have Had An Inadequate Response To Conventional Therapy.,Infliximab Is Indicated For Reducing Signs And Symptoms, Inducing And Maintaining Clinical Remission And Mucosal Healing, And Eliminating Corticosteroid Use In Adult Patients With Moderately To Severely Active Ulcerative Colitis Who Have Had An Inadequate Response To Conventional Therapy.,Infliximab Is Indicated For Reducing Signs And Symptoms And Inducing And Maintaining Clinical Remission In Pediatric Patients 6 Years Of Age And Older With Moderately To Severely Active Ulcerative Colitis Who Have Had An Inadequate Response To Conventional Therapy.,Infliximab, In Combination With Methotrexate, Is Indicated For Reducing Signs And Symptoms, Inhibiting The Progression Of Structural Damage, And Improving Physical Function In Patients With Moderately To Severely Active Rheumatoid Arthritis.,Infliximab Is Indicated For Reducing Signs And Symptoms In Patients With Active Ankylosing Spondylitis.,Infliximab Is Indicated For Reducing Signs And Symptoms Of Active Arthritis, Inhibiting The Progression Of Structural Damage, And Improving Physical Function In Patients With Psoriatic Arthritis.,Infliximab Is Indicated For The Treatment Of Adult Patients With Chronic Severe (I.E., Extensive And/Or Disabling) Plaque Psoriasis Who Are Candidates For Systemic Therapy And When Other Systemic Therapies Are Medically Less Appropriate. 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Aminosteril N Hepa 8% [80.000 Mg/Ml] Solution   For Infusion) Is For Supply Of Amino Acids As Part Of A Parenteral Nutrition Regimen In Severe Forms Of Hepatic Insufficiency With And Without Hepatic Encephalopathy When Oral Or Enteral Nutrition Is Impossible Or Insufficient Or Contraindicated.","dt_closure_dt":"24-FEB-2021","str_man_unit_name":"Fresenius Kabi India Pvt. Ltd."},{"str_drug_name":"Intravenous Amino Acids Solution 10% For Infant","str_composition":"L-Isoleucine 8.0000 Gm/1000ml,L-Leucine 13.0000 Gm/1000ml,L-Lysine Monoacetate 12.00 G Corresponding To L-Lysine 8.5100 Gm/1000ml,L-Methionine 3.1200 Gm/1000ml,N-Acetyl-L-Cysteine 0.700 G Corresponding To L-Cysteine 0.5200 Gm/1000ml,L-Phenylalanine 3.7500 Gm/1000ml,L-Threonine 4.4000 Gm/1000ml,L-Tryptophan 2.0100 Gm/1000ml,L-Valine 9.0000 Gm/1000ml,L-Arginine 7.5000 Gm/1000ml,L-Histidine 4.7600 Gm/1000ml,Glycine 4.1500 Gm/1000ml,L-Alanine 9.3000 Gm/1000m,L-Proline 9.7100 Gm/1000ml,L-Serine 7.6700 Gm/1000ml,Taurine 0.4000 Gm/1000ml,N-Acetyl-L-Tyrosine 5.176 G Corresponding To L-Tyrosine 4.2000 Gm/1000ml,L-Malic Acid 2.6200 Gm/1000ml","str_indication":"Intravenous Amino Acids Solution 10% For Infant (Brand Name ? 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Ltd."},{"str_drug_name":"Intravenous Amino Acids Solution For Infusion","str_composition":"L-Isoleucine 5.1000 Gm/1000ml,L-Leucine 10.3000 Gm/1000ml,L-Lysine Monoacetate 10.01 G Corresponding To L-Lysine 7.1000 Gm/1000ml,L-Methionine 2.8000 Gm/1000ml,N-Acetyl-L-Cysteine 0.50 G Corresponding To L-Cysteine 0.3700 Gm/1000ml,L-Phenylalanine 3.8000 Gm/1000ml,L-Threonine 4.8000 Gm/1000ml,L-Tryptophan 1.9000 Gm/1000ml,L-Valine 6.2000 Gm/1000ml,L-Arginine 4.9000 Gm/1000ml,L-Histidine 4.3000 Gm/1000ml,Glycine 3.2000 Gm/1000ml,L-Alanine 6.3000 Gm/1000ml,L-Proline 4.3000 Gm/1000ml,L-Serine 4.5000 Gm/1000ml,L-Malic Acid 1.5000 Gm/1000ml,Glacial Acetic Acid 1.3800 Gm/1000ml","str_indication":"Intravenous Amino Acids Solution For Infusion (Brand Name: Nephrosteril 70.00 Mg/Ml Solution For Infusion) Is Balanced Supply Of Protein Elements In Acute And Chronic Renal Insufficiency As Well As During Peritoneal And Hemodialysis Treatment.","dt_closure_dt":"22-MAR-2021","str_man_unit_name":"Fresenius Kabi India Pvt. 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Q.s or q.s, energy content-1058 kcal/lit or 1908 kcal/lit, osmolarity-345 Mos mol/lit or 380 Mos moޡ\u0005","str_indication":"For patients requiring parental nutrition in energy depletion as well as essential fatty acid deficiency states.","dt_closure_dt":"11/07/2001","str_man_unit_name":"Core health care ltd."},{"str_drug_name":"Iobenzamic acid","str_composition":"","str_indication":"Oral cholecystography","dt_closure_dt":"1965- August","str_man_unit_name":"May & Bakers, Bombay"},{"str_drug_name":"Iobitridol soln for inj.","str_composition":"Each ml contains; iobitridol corresponding to 250mg, 300mg, 350mg of iodine.","str_indication":"For patients undergoing i.v urography, barin & whole body CT, digital substraction angiography of aorta & lower limbs & angio cardiography.","dt_closure_dt":"17-10-2001","str_man_unit_name":"Choksai brothers p ltd."},{"str_drug_name":"Iobitridol Solution for Injection Each 100mg solution contain 65.81 g Iobitridol corressponding mass of Iodine 30gm","str_composition":"","str_indication":"By intracavity route for Arthrography and Hysterosalpingography.","dt_closure_dt":"19.03.13","str_man_unit_name":""},{"str_drug_name":"Iodamide","str_composition":"300/350","str_indication":"300-intravenous urography, 350-angiocardiography.","dt_closure_dt":"1967- October","str_man_unit_name":"Pharrmed Pvt ltd, Bombay"},{"str_drug_name":"Iodixanol Injection","str_composition":"Each ml contains:\r\nIodixanol 652 mg equivalent to 320 mg I.\r\nIodixanol 305 mg equivalent to 150 mg I.\r\nIodixanol 550 mg equivalent to 270 mg I.","str_indication":"NA","dt_closure_dt":"23 September 1999","str_man_unit_name":"Anita Enterprises"},{"str_drug_name":"Iohexol","str_composition":"Iohexol 0.0000 Not Applicable (Na)","str_indication":"NA","dt_closure_dt":"28-JAN-2025","str_man_unit_name":"Deep Shell Enterprise"},{"str_drug_name":"Iohexol Injection","str_composition":"Sodium Calcium Edetate 0.1000 Mg/Ml,Water For Injections 0.6500 Ml,Hydrochloric Acid 5 N To Ph 6.8 - 7.6 1.4000 ?l,Iohexol 350mgi/Ml 755.0000 Mg/Ml,Trometamol 1.2100 Mg/Ml","str_indication":"Contrast Enhanced Spectral Mammography","dt_closure_dt":"20-MAR-2026","str_man_unit_name":"Wipro GE Healthcare Pvt. 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Ltd."},{"str_drug_name":"Iopromide Injection U.S.P.","str_composition":"Iopromide 0.6230 Gram (G)","str_indication":"Contrast Mammography to visualize known or suspected lesions of the breast in adults, as an adjunct following mammography and/or ultrasound","dt_closure_dt":"16-FEB-2026","str_man_unit_name":"Bayer Pharmaceuticals Pvt. Ltd."},{"str_drug_name":"Ioversol injection (finished formulation)","str_composition":"160,240,300,320,350","str_indication":"Contrast medium","dt_closure_dt":"29/12/1993","str_man_unit_name":"J.B.Chemicals & Pharma, Bombay"},{"str_drug_name":"Ipilimumab","str_composition":"Ipilimumab 53.5000 Milligram (Mg),Tris Hydrochloride 33.7000 Milligram (Mg),Sodium Chloride 62.6000 Milligram (Mg),Mannitol 107.0000 Milligram (Mg),Pentetic Acid 0.4200 Milligram (Mg),Polysorbate 80 1.1800 Milligram (Mg),Sodium Hydroxide 0.0000 Qs To Ph 7,Hydrochloric Acid 0.0000 Qs To Ph 7,Water For Injection 10.7000 Ml (Qs),Each Vial Includes 0.7000 Ml Overfill For Vial Needle Syringe (Vns) Holdup","str_indication":"Renal Cell Carcinoma (Rcc) - Ipilimumab Is Indicated For Treatment Of Patients With Intermediate Or Poor Risk, Previously Untreated Advanced Renal Cell Carcinoma, In Combination With Nivolumab.","dt_closure_dt":"24-FEB-2020","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Ipilimumab","str_composition":"Tris Hydrochloride 33.7000 Milligram (Mg),Ipilimumab 53.5000 Milligram (Mg),Water For Injection 0.0000 Q.S. To 10.7 Ml,Nitrogen 0.0000 Not Applicable (Na),Sodium Chloride 62.6000 Milligram (Mg),Mannitol 107.0000 Milligram (Mg),Sodium Hydroxide 0.0000 Q.S. To Ph 7.0,Hydrochloric Acid 0.0000 Q.S. To Ph 7.0,Polysorbate 80 1.1800 Milligram (Mg),Pentetic Acid 0.4200 Milligram (Mg)","str_indication":"Esophageal Cancer- Ipilimumab, In Combination With Nivolumab, Is Indicated For The First-Line Treatment Of Adult Patients With Unresectable Advanced Or Metastatic Esophageal Squamous Cell Carcinoma (Escc)","dt_closure_dt":"25-OCT-2024","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Ipilimumab 5 Mg/Ml Concentrate For Solution For Infusion (50mg/10ml)","str_composition":"Ipilimumab 53.5000 Mg/Vial,Tris Hydrochloride 33.7000 Mg/Vial,Sodium Chloride 62.6000 Mg/Vial,Mannitol 107.0000 Mg/Vial,Pentetic Acid 0.4200 Mg/Vial,Polysorbate 80 1.1800 Mg/Vial,Sodium Hydroxide 0.0000 Q.S. To Ph 7.0,Hydrochloric Acid 0.0000 Q.S. To Ph 7.0,Water For Injection 0.0000 Q.S. To 10.7ml,Nitrogen 0.0000 Not Applicable","str_indication":"Unresectable Or Metastatic Melanoma - Ipilimumab, In Combination With Nivolumab, Is Indicated For The Treatment Of Unresectable Or Metastatic Melanoma In Adult Patients,Hepatocellular Carcinoma - Ipilimumab, In Combination With Nivolumab, Is Indicated For The First-Line Treatment Of Adult Patients With Unresectable Or Metastatic Hepatocellular Carcinoma (Hcc).","dt_closure_dt":"19-DEC-2025","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Ipilimumab 5 Mg/Ml Concentrate For Solution For Infusion (50mg/10ml)","str_composition":"Ipilimumab 53.5000 Mg/Vial,Hydrochloric Acid 0.0000 Q.S. To Ph 7.0,Sodium Hydroxide 0.0000 Q.S. To Ph 7.0,Mannitol 107.0000 Mg/Vial,Water For Injection 0.0000 Q.S. 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Ltd."},{"str_drug_name":"Ipratropium bromide inhaler","str_composition":"Each actuation delivers; ipratropium bromide-20 mcg.","str_indication":"Anti chlonergic bronchodilator- Chronic obstructive bronchitis, emphysema, bronchospasm, during and after surgery and moderate to asthmatic attacks in chronic form of asthma.","dt_closure_dt":"20/11/1992","str_man_unit_name":"Cipla"},{"str_drug_name":"Ipratropium bromide respirator solution/nasal spray","str_composition":"Ipratropium bromide respirator solution-250mcg/ml, ipratropium bromide nasal spray each actuation delivers-20mcg.","str_indication":"","dt_closure_dt":"08/04/1993","str_man_unit_name":"Cipla"},{"str_drug_name":"Ipratropium bromide + salbutamol sulphate","str_composition":"Each actuation delivers; salbutamol sulphate eq.to salbutamol-100mg, ipratropium bromide BP-20mcg","str_indication":"In treatment of chronic obstructive pulmonary disease.","dt_closure_dt":"06/03/2000","str_man_unit_name":"Cipla ltd."},{"str_drug_name":"Ipratropium bromide + salbutamol sulphate","str_composition":"Each 2.5ml contains; ipratropium bromide-500mcg, salbutamol sulphate eq.to salbutamol-2.5mg","str_indication":"By RMP- for bronchospasm in patients suffering from chronic pulmonary disorders.","dt_closure_dt":"03/04/2001","str_man_unit_name":"Cipla ltd."},{"str_drug_name":"Irbesartan","str_composition":"Each uncoated tablet contains; irbesartan-75mg,150mg,300mg","str_indication":"By RMP- for the treatment of mild to moderate hypertension only.","dt_closure_dt":"26-06-2000","str_man_unit_name":"Sun pharma (bulk=formulation)"},{"str_drug_name":"Irbesartan + hydrochlorthiazide ","str_composition":"Each uncoated tablet contains; irbesartan-150mg,300mg, Hydrochlorthiazide-12.5mg","str_indication":"By RMP- for mild to moderate hypertension.","dt_closure_dt":"31-01-2001","str_man_unit_name":"Sun pharmaceuticals ltd."},{"str_drug_name":"Irinotecan HCl Trihydrate Injection 20 mg/ml (Pack Size 25ml)","str_composition":"","str_indication":"For the treatment of metastatic colorectal cancer.","dt_closure_dt":"31.08.10","str_man_unit_name":""},{"str_drug_name":"Irinotecan hcl trihydrate solution for i.v infusion","str_composition":"Each 2ml solution contains; irinotecan hcl trihydrate-40mg, Each 5ml solution contains; irinotecan hcl trihydrate-100mg","str_indication":"Anticancer-For the treatment of colo-rectal cancer.","dt_closure_dt":"23-05-1997 to 22-05-1999","str_man_unit_name":"Rhone poulenc"},{"str_drug_name":"Iron Amino Acid Chelate as Ferrous Bisglycinate (75mg) eq. to Elemental Iron 15mg + Folic acid IP 0.25mg + Vitamin B 12 IP 3.75mcg + Zinc Picolinate (26mg) eq. To elemental zinc 5.5mg syrup","str_composition":"","str_indication":"For the treatment of Iron Deficiency Anaemia.","dt_closure_dt":"22.12.11","str_man_unit_name":""},{"str_drug_name":"Iron dextran glycoside","str_composition":"5 & 10 ml ampl.","str_indication":"iron deficiency anaemia.","dt_closure_dt":"1967- June","str_man_unit_name":"Martin & Harris, Bombay"},{"str_drug_name":"Iron (III) isomaltoside 1000 solution for injection/infusion 100mg per ml","str_composition":"Each ml contains; Iron (III) isomaltoside 1000-100mg","str_indication":"For the treatment of iron deficiency anaemia when oral iron preparations are ineffective or cannot be used and when there is a clinical need to deliver iron rapidly.","dt_closure_dt":"20.08.13","str_man_unit_name":"Max Neeman medical international ltd."},{"str_drug_name":"Iron polymaltose","str_composition":"2ml=100mg Fe","str_indication":"Antianaemia-iron therapy.","dt_closure_dt":"1963- April","str_man_unit_name":"Khandelwal lab, Bombay"},{"str_drug_name":"Iron sorbitol citric acid complex","str_composition":"Each ml contains eq.of 50mg of Iron as iron sorbitol citric acid complex.","str_indication":"","dt_closure_dt":"1969- July","str_man_unit_name":"Hyba labs, bombay"},{"str_drug_name":"Iron-sorbitol citric acid complex","str_composition":"2ml (50mgFe+++)","str_indication":"Haematinic-Parentral iron (Colloidal iron complex).","dt_closure_dt":"1962- May","str_man_unit_name":"British drug thomson, Bombay"},{"str_drug_name":"Iron sorbitol citric acid complex (Injection of colloidal iron)","str_composition":"","str_indication":"","dt_closure_dt":"1969- January","str_man_unit_name":"Croobs, Bombay"},{"str_drug_name":"Iron sucrose complex inj. i.v (finished formulation)","str_composition":"","str_indication":"All cases of iron deficiency in which rapid and reliable substitution of iron is required.","dt_closure_dt":"02/01/1999","str_man_unit_name":"Emcure pharma"},{"str_drug_name":"Iron sucrose injection","str_composition":"Eacg 5ml contains; iron (as iron sucrose)-100mg","str_indication":"Indicated in iron deficiency anemia in which rapid and reliable substitution of iron is required.","dt_closure_dt":"25/03/2004","str_man_unit_name":"Hetero drug ltd."},{"str_drug_name":"Irsogladine Maleate Tablet  2mg /4mg","str_composition":"Each uncoated tablet contains; irsogladine maleate-2mg, 4mg","str_indication":"For gastric ulcers, improvement of gastric mucosal lesion (erosion, hemorrhage, redness and edema) caused by acute gastritis and acute exacerbation stage of chronic gastritis.","dt_closure_dt":"10.05.10","str_man_unit_name":"Macleods pharma, Mumbai"},{"str_drug_name":"Isapterl-II","str_composition":"Prepared from granulated Plantago ovata(Isapgol) seed husk (IP) and effervescent powder","str_indication":"","dt_closure_dt":"1981-March","str_man_unit_name":"CDRI Lucknow"},{"str_drug_name":"Isavuconazole Capsules 100 Mg","str_composition":"Isavuconazonium Sulfate 186.3000 Milligram (Mg)","str_indication":"Indicated For Patients 18 Years Of Age And Older For The Treatment Of Invasive Aspergillosis And Invasive Mucormycosis","dt_closure_dt":"06-SEP-2023","str_man_unit_name":"BDR Pharmaceuticals International Pvt Ltd"},{"str_drug_name":"Isavuconazole For Injection 200 Mg","str_composition":"Isavuconazonium Sulfate Equivalant To  Isavuconazole 200.0000 Milligram (Mg)","str_indication":"Indicated For Patients 18 Years Of Age And Older For The Treatment Of Invasive Aspergillosis And Invasive Mucormycosis","dt_closure_dt":"29-MAR-2022","str_man_unit_name":"GUFIC BIOSCIENCES LIMITED"},{"str_drug_name":"Isavuconazole Sulfate","str_composition":"Isavuconazole Sulfate Equivalent To Isavuconazole 200.0000 Milligram (Mg)","str_indication":"Isavuconazole Is An Azole Antifungal Indicated For Patients 18 Years Of Age And Older For The Treatment Of Invasive Aspergillosis And Invasive Mucormycosis","dt_closure_dt":"01-MAY-2020","str_man_unit_name":"Pfizer Products India Private Limited "},{"str_drug_name":"Isavuconazole Sulfate","str_composition":"Isavuconazole Sulfate Equivalent To Isavuconazole 100.0000 Milligram (Mg)","str_indication":"Isavuconazole Sulfate Is An Azole Antifungal Indicated For Patients 18 Years Of Age And Older For The Treatment Of Invasive Aspergillosis And Invasive Mucormycosis","dt_closure_dt":"18-FEB-2020","str_man_unit_name":"Pfizer Products India Private Limited "},{"str_drug_name":"Isavuconazonium Sulfate","str_composition":"Isavuconazonium Sulfate 200.0000 Milligram (Mg)","str_indication":"NA","dt_closure_dt":"29-MAR-2022","str_man_unit_name":"GUFIC BIOSCIENCES LIMITED"},{"str_drug_name":"Isavuconazonium Sulphate","str_composition":"Isavuconazonium Sulphate 97.0000 %","str_indication":"NA","dt_closure_dt":"14-NOV-2022","str_man_unit_name":"Virdev Intermediates Pvt. Ltd."},{"str_drug_name":"Isavuconazonium Sulphate","str_composition":"Isavuconazonium Sulphate 334.8000 Milligram (Mg)","str_indication":"Indicated For Patients 18 Years Of Age And Older For The Treatment Of Invasive Aspergillosis And Invasive Mucormycosis","dt_closure_dt":"16-NOV-2022","str_man_unit_name":"BDR Pharmaceuticals International Pvt Ltd"},{"str_drug_name":"Isavuconazonium Sulphate","str_composition":"Amino Impurity 0.1500 %W/W,Oxazin Impurity 0.1500 %W/W,Methyl Ester Impurity 0.1500 %W/W,Isavuconazonium Methyl Hydroxy Impurity 0.5000 %W/W,Isavuconazole 0.1500 %W/W,Boc Isavuconazonium 0.1500 %W/W,Di N Methyl Ester Impurity 0.1500 %W/W,Highest Individual Unspecified Impurity 0.1000 %W/W,Total Impurities 1.0000 %W/W,Isavuconazonium Sulfate 98.0000 %W/W","str_indication":"NA","dt_closure_dt":"19-FEB-2025","str_man_unit_name":"M/s METROCHEM API PVT LTD - UNIT-IV"},{"str_drug_name":"Isepamicin injection","str_composition":"Each ml contains; isepamicin sulfate eq.to 100mg,250mg of isepamicin.","str_indication":"LRTI, intra abdominal infection, UTI, skin & soft tissue infection and septicemia.","dt_closure_dt":"26-12-1997 to 26-12-1999","str_man_unit_name":"Fulford ltd."},{"str_drug_name":"Isepamicin Sulfate Jp","str_composition":"Isepamicin Sulfate 100.0000 Mg/Ml","str_indication":"NA","dt_closure_dt":"25-OCT-2021","str_man_unit_name":"APC Pharmaceuticals And Chemicals"},{"str_drug_name":"ISMN 30mg SR + Atenolol 50mg tablets (Additional Strength)","str_composition":"","str_indication":"Same as Approved.","dt_closure_dt":"19.03.08","str_man_unit_name":""},{"str_drug_name":"ISMN 30mg SR + Metoprolol Succinate equivalent to metoprolol tartrate 25mg/50mg tablets (Additional Strength)","str_composition":"","str_indication":"Same as Approved","dt_closure_dt":"02.01.08","str_man_unit_name":""},{"str_drug_name":"ISMN 60mg Sr + Atenolol 50mg/100mg","str_composition":"","str_indication":"For angina pectoris","dt_closure_dt":"23.03.07","str_man_unit_name":""},{"str_drug_name":"ISMN SR 30mg + Aspirin75/150mg tablet (addl. 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(3) Musculoskeletal conditions. (4) Shock. (5) Parturient paresis (supportivޡ\u0005","dt_closure_dt":"03.10.09 ","str_man_unit_name":""},{"str_drug_name":"Isoflurane","str_composition":"","str_indication":"Used for induction and maintenance of general anaesthesia.","dt_closure_dt":"1990-July","str_man_unit_name":"Abbott lab, Bombay"},{"str_drug_name":"Isometamidium Chloride","str_composition":"","str_indication":"Indicated in treatment of cardiac arrhythmias including atrial fibrillation, ventricular tachycardia, arrhythmia.","dt_closure_dt":"1977-January","str_man_unit_name":"May & Baber"},{"str_drug_name":"Isoniazid 300mg+Rifapentine 300mg","str_composition":"Rifapentine 270.0000 Milligram (Mg),Isoniazid 270.0000 Milligram (Mg)","str_indication":"Indicated In The Treatment Of Pulmonary Tuberculosis.","dt_closure_dt":"27-NOV-2024","str_man_unit_name":"Themis Medicare Ltd."},{"str_drug_name":"Isoniazid 300mg+Rifapentine 300mg","str_composition":"Isoniazid 300mg 98.0000 %,Rifapentine 300mg 98.0000 %W/W","str_indication":"Indicated For Treatment Of Latent Tuberculosis, Caused By Mycobacterium Tuberculosis (For Use In Ntep Only)","dt_closure_dt":"06-SEP-2023","str_man_unit_name":"J Duncan Healthcare Pvt. 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SIONC PHARMACEUTICALS PRIVATE LIMITED"},{"str_drug_name":"Nitisinone","str_composition":"Nitisinone 2.0000 Milligram (Mg)","str_indication":"Heredityary Tyrosinemia Type -I (Ht-1)","dt_closure_dt":"14-JUN-2024","str_man_unit_name":"BRAWN LABORATORIES LIMITED"},{"str_drug_name":"Nitisinone Capsules","str_composition":"Nitisinone 2.0000 Milligram (Mg)","str_indication":"Nitisinone Capsules Is Indicated For The Treatment Of Adult And Pediatric Patients With Hereditary Tyrosinemia Type 1 (Ht-1) In Combination With Dietary Restriction Of Tyrosine And Phenylalanine.","dt_closure_dt":"10-JAN-2023","str_man_unit_name":"Zenara Pharma Private Limited"},{"str_drug_name":"Nitisinone Capsules","str_composition":"Nitisinone 20.0000 Milligram (Mg)","str_indication":"Nitisinone Capsules Is Indicated For The Treatment Of Adult And Pediatric Patients With Hereditary Tyrosinemia Type 1 (Ht-1) In Combination With Dietary Restriction Of Tyrosine And Phenylalanine.","dt_closure_dt":"10-JAN-2023","str_man_unit_name":"Zenara Pharma Private Limited"},{"str_drug_name":"Nitisinone Capsules","str_composition":"Nitisinone 10.0000 Milligram (Mg)","str_indication":"Nitisinone Capsules Is Indicated For The Treatment Of Adult And Pediatric Patients With Hereditary Tyrosinemia Type 1 (Ht-1) In Combination With Dietary Restriction Of Tyrosine And Phenylalanine.","dt_closure_dt":"10-JAN-2023","str_man_unit_name":"Zenara Pharma Private Limited"},{"str_drug_name":"Nitisinone Capsules","str_composition":"Nitisinone 5.0000 Milligram (Mg)","str_indication":"Nitisinone Capsules Is Indicated For The Treatment Of Adult And Pediatric Patients With Hereditary Tyrosinemia Type 1 (Ht-1) In Combination With Dietary Restriction Of Tyrosine And Phenylalanine.","dt_closure_dt":"10-JAN-2023","str_man_unit_name":"Zenara Pharma Private Limited"},{"str_drug_name":"Nitisinone Capsules 2 Mg, 5 Mg And 10 Mg","str_composition":"Nitisinone 5.0000 Milligram (Mg)","str_indication":"Indicated For The Treatment Of Adult And Paediatric In Any Age Range Patients With Confirmed Diagnosis Of Hereditary Tyrosinemia Type 1 Ht 1 In Combination With Dietary Restriction Of Tyrosine And Phenylalanine And Treatment Of Adult Patients With Alkaptonuria.","dt_closure_dt":"12-JUL-2022","str_man_unit_name":"LAURUS LABS LIMITED"},{"str_drug_name":"Nitisinone Capsules 2 Mg, 5 Mg And 10 Mg","str_composition":"Nitisinone 2.0000 Milligram (Mg)","str_indication":"Indicated For The Treatment Of Adult And Paediatric In Any Age Range Patients With Confirmed Diagnosis Of Hereditary Tyrosinemia Type 1 Ht 1 In Combination With Dietary Restriction Of Tyrosine And Phenylalanine And Treatment Of Adult Patients With Alkaptonuria.","dt_closure_dt":"12-JUL-2022","str_man_unit_name":"LAURUS LABS LIMITED"},{"str_drug_name":"Nitisinone Capsules 2 Mg, 5 Mg And 10 Mg","str_composition":"Nitisinone 10.0000 Milligram (Mg)","str_indication":"Indicated For The Treatment Of Adult And Paediatric In Any Age Range Patients With Confirmed Diagnosis Of Hereditary Tyrosinemia Type 1 Ht 1 In Combination With Dietary Restriction Of Tyrosine And Phenylalanine And Treatment Of Adult Patients With Alkaptonuria.","dt_closure_dt":"12-JUL-2022","str_man_unit_name":"LAURUS LABS LIMITED"},{"str_drug_name":"Nitisinone Tablets 10mg","str_composition":"Nitisinone 10.0000 Milligram (Mg)","str_indication":"For The Treatment Of Hereditary Tyrosinemia Type 1 (Ht-1),For  The  Treatment  Of  Adult Patients   With   Alkaptonuria(Aku)","dt_closure_dt":"21-AUG-2025","str_man_unit_name":"BRAWN LABORATORIES LIMITED"},{"str_drug_name":"Nitrazepam","str_composition":"Each tablet contains; Nitrazepam-5mg","str_indication":"","dt_closure_dt":"1973-September","str_man_unit_name":"Ranbaxy"},{"str_drug_name":"Nitrazepam","str_composition":"","str_indication":"Epileptic","dt_closure_dt":"1973-June","str_man_unit_name":"Ranbaxy, La-Medica, Unique pharmaceutica, Pharmaceutical Co"},{"str_drug_name":"Nitrendipine","str_composition":"Each tablet contains; nitrendipine-10mg,20mg","str_indication":"Anti hypertensive- In the treatment of mild to moderate hypertension.","dt_closure_dt":"1991- May","str_man_unit_name":"U.S. Vitamin"},{"str_drug_name":"Nitrendipine + Atenolol tabs","str_composition":"Each tab contains; nitrendipine-10mg,20mg, atenolol-30mg","str_indication":"Mild to  moderate hypertension not responding to monotherapy with either of the drug.","dt_closure_dt":"19/09/1995","str_man_unit_name":""},{"str_drug_name":"Nitric Oxide Nasal Spray","str_composition":"Nitric Oxide 0.2000 Ppm Hr Per Ml","str_indication":"For Use As A Mechanical And Chemical Barrier That Protects Against Respiratory Viruses (Such As Sars Cov-2) Inside The Nasal Cavity.","dt_closure_dt":"18-FEB-2022","str_man_unit_name":"Glenmark Pharmaceuticals Ltd."},{"str_drug_name":"Nitrofurantoin BP","str_composition":"Each Disc is in pregnated with Nitrofurantoin BP-100mcg, 200mcg","str_indication":"","dt_closure_dt":"1974-March","str_man_unit_name":"SKF Bangulore"},{"str_drug_name":"Nitrofurantoin dispersible tablets 50 mg (add. Strength/ dosage form)","str_composition":"","str_indication":"For the treatment of acute uncomplicated urinary tract infections (acute cystitis) caused by susceptible strains of E.coli or staphylococcus saprophyticus.","dt_closure_dt":"15.12.14","str_man_unit_name":""},{"str_drug_name":"Nitrofurantoin SR Tab. 100mg","str_composition":"Each film coated sustained release tablet contains; nitrofurantoin BP-100mg","str_indication":"For the treatment of acute uncomplicated urinary tract infections (acute cystitis) caused by susceptible strains of Escherichia coli or Staphylococcus saprophyticus.","dt_closure_dt":"01.10.08","str_man_unit_name":"Intas pharma, Ahmedabad"},{"str_drug_name":"Nitrofurazone + Urea","str_composition":"Each bolus contains; Nitrofurazone-0.06gm, Urea-6.21gm","str_indication":"","dt_closure_dt":"1973-August","str_man_unit_name":"SKF Bangulore"},{"str_drug_name":"Nitroglycerine","str_composition":"Each sustained release tablet contains; nitroglycerine-2.6mg","str_indication":"","dt_closure_dt":"1975-March","str_man_unit_name":"Sarabhai chemicals,Baroda"},{"str_drug_name":"Nitroglycerine in 5% dextrose inj.","str_composition":"Each 100ml contain; nitroglycerine-10mg,20mg,40mg, dextrose hydrous-5gm","str_indication":"For treatment of perioperative hypertension for control of congestive heart failure in setting of acute MI, angina pectoris in patients who have not responded to sublingual nitroglycerine & beta blockers & for indication of intraoperative hypotension.","dt_closure_dt":"02/04/2002","str_man_unit_name":"Baxter India ltd."},{"str_drug_name":"Nitroglycerin injection","str_composition":"","str_indication":"Cardiac drug- Indicated in the treatment of angina pectoris, myocardial infarction etc.","dt_closure_dt":"1986-June","str_man_unit_name":"Walter bushnell"},{"str_drug_name":"Nitroglycerin oitnment","str_composition":"","str_indication":"Anti-anginal drug- Indicated in treatment of angina pectoris due to coronary artery disease.","dt_closure_dt":"1982-january","str_man_unit_name":"Arun & C0., Bombay"},{"str_drug_name":"Nitroglycerin patches (finished formulation)","str_composition":"Each patch contains; nitroglycerin-25mg,50mg","str_indication":"For the treatment of angina pectoris due to coronary artery disease.","dt_closure_dt":"03/06/1993","str_man_unit_name":"Hindustan ciba geigy ltd."},{"str_drug_name":"Nitroscanate tablets","str_composition":"Each tablet contains; nitroscanate-100mg,500mg","str_indication":"For control/eradication of hook worms/round worms/tape worms in puppies and adult dogs.","dt_closure_dt":"19/02/1996","str_man_unit_name":"Hindustan ciba geigy ltd."},{"str_drug_name":"Nitrous oxide as pre mixed gases","str_composition":"Homogenous gas containing 50% nitrous oxide by volume & 50% oxygen by volume compressed in a cylinder.","str_indication":"For relief of pain usually in emergency situation & several in vasive procedure.","dt_closure_dt":"20/12/2001","str_man_unit_name":"BOC India ltd."},{"str_drug_name":"Nitroxazepine Hydrochloride","str_composition":"Each 2mL contains; Sitamil-25mg(Nitroxazepine Hydrochloride), Each tablet contains; Sitamil-25mg(Nitroxazepine Hydrochloride)","str_indication":"Developed in India.","dt_closure_dt":"1973-September/ October","str_man_unit_name":"Ciba of India, Bombay"},{"str_drug_name":"Nivolumab","str_composition":"Sodium Hydroxide 0.0000 Q.S. To Ph 6.0,Pentetic Acid 0.0370 Milligram (Mg),Water For Injection 0.0000 Q.S. To 4.7 Ml,Mannitol 141.0000 Milligram (Mg),Sodium Citrate, Dihydrate 27.6000 Milligram (Mg),Hydrochloric Acid 0.0000 Q.S. To Ph 6.0,Polysorbate 80 0.9400 Milligram (Mg),Nivolumab 47.0000 Milligram (Mg),Each Vial Includes A 0.7 Ml Overfill For Vial, Needle, And Syringe (Vns) Holdup 0.7000 Ml,Sodium Chloride 13.7000 Milligram (Mg)","str_indication":"Nivolumab Is Indicated For The Adjuvant Treatment Of Completely Resected Esophageal Or Gastroesophageal Junction Cancer With Residual Pathologic Disease In Patients , Who Have Received Neoadjuvant Chemoradiotherapy (Crt).,Nivolumab, In Combination With Fluoropyrimidine- And Platinum-Containing Chemotherapy, Is Indicated For The Treatment Of Patients With Advanced Or Metastatic Gastric Cancer, Gastroesophageal Junction Cancer, And Esophageal Adenocarcinoma.","dt_closure_dt":"30-NOV-2021","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Nivolumab 107.0000 Milligram (Mg),Sodium Citrate, Dihydrate 62.9000 Milligram (Mg),Sodium Chloride 31.2000 Milligram (Mg),Mannitol 321.0000 Milligram (Mg),Pentetic Acid 0.0856 Milligram (Mg),Polysorbate 80 2.1400 Milligram (Mg),Hydrochloric Acid 0.0000 Q.S. To Ph 6.0,Sodium Hydroxide 0.0000 Q.S. To Ph 6.0,Water For Injection 0.0000 Q.S. To 10.7 Ml,Each Vial Includes A 0.7 Ml Overfill For Vial, Needle, And Syringe (Vns) Holdup. 0.7000 Ml","str_indication":"Nivolumab Is Indicated For The Treatment Of Patients With Unresectable Advanced, Recurrent, Or Metastatic Esophageal Squamous Cell Carcinoma (Escc) After Prior Fluoropyrimidine- And Platinum-Based Chemotherapy.","dt_closure_dt":"04-AUG-2021","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Sodium Citrate, Dihydrate 147.0000 Milligram (Mg),Mannitol 750.0000 Milligram (Mg),Nivolumab 250.0000 Milligram (Mg),Water For Injection 0.0000 Q.S To 25 Ml,Sodium Chloride 73.0000 Milligram (Mg),Sodium Hydroxide 0.0000 Q.S To Ph 6.0,Hydrochoric Acid 0.0000 Q.S To Ph 6.0,Polysorbate 80 5.0000 Milligram (Mg),Pentetic Acid 0.2000 Milligram (Mg)","str_indication":"Non-Small Cell Lung Cancer (Nsclc): Nivolumab As A Single Agent Is Indicated For The Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) After Prior Chemotherapy. Nivolumab, In Combination With Ipilimumab And 2 Cycles Of Platinum-Doublet Chemotherapy, Is Indicated For The First-Line Treatment Of Adult Patients With Metastatic Or Recurrent Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations.,Renal Cell Carcinoma (Rcc):  Nivolumab As A Single Agent Is Indicated For The Treatment Of Patients With Advanced Renal Cell Carcinoma (Rcc) After Prior Therapy In Adults. Nivolumab Is Indicated For The Treatment Of Patients With Intermediate Or Poor Risk, Previously Untreated Advanced Renal Cell Carcinoma, In Combination With Ipilimumab.,Squamous Cell Carcinoma Of The Head And Neck (Scchn):  Nivolumab As Monotherapy Is Indicated For The Treatment Of Recurrent Or Metastatic Squamous Cell Carcinoma Of The Head And Neck After Platinum-Based Therapy.,Melanoma:  Nivolumab As A Single Agent Is Indicated For The Treatment Of Patients With Braf V600 Wildtype Unresectable Or Metastatic Melanoma. Nivolumab As A Single Agent Is Indicated For The Treatment Of Patients With Braf V600 Mutation Positive Unresectable Or Metastatic Melanoma.  Nivolumab Is Indicated For The Treatment Of Patients With Melanoma With Lymph Node Involvement Or Metastatic Disease Who Have Undergone Complete Resection, In The Adjuvant Setting.,Classical Hodgkin Lymphoma (Chl):  Nivolumab Is Indicated For The Treatment Of Adult Patients With Classical Hodgkin Lymphoma (Chl) That Has Relapsed Or Progressed After Autologous Hematopoietic Stem Cell Transplantation (Hsct) And Brentuximab Vedotin, Or 3 Or More Lines Of Systemic Therapy That Includes Autologous Hsct,Urothelial Carcinoma (Uc): Nivolumab Is Indicated For The Treatment Of Patients With Locally Advanced Or Metastatic Urothelial Carcinoma Who Have Disease Progression During Or Following Platinum-Containing Chemotherapy And?Have Disease Progression Within 12 Months Of Neoadjuvant Or Adjuvant Treatment With Platinum-Containing Chemotherapy.,Colorectal Cancer (Crc):  Nivolumab As Montherapy Is Indicated For The Treatment Adult And Pediatric (12 Years And Older) Patients With Microsatellite Instability-High (Msi-H) Or Mismatch Repair Deficient (Dmmr) Metastatic Colorectal Cancer That Has Progressed Following Treatment With A Fluoropyrimidine, Oxaliplatin, And Irinotecan, As A Single Agent.,Esophageal Squamous Cell Carcinoma (Escc):  Nivolumab Is Indicated For The Treatment Of Patients With Unresectable Advanced, Recurrent, Or Metastatic Esophageal Squamous Cell Carcinoma (Escc) After Prior Fluoropyrimidine- And Platinum-Based Chemotherapy.,Gastric Cancer, Gastroesophageal Junction Cancer, And Esophageal Adenocarcinoma (Gc, Gejc Or Eac):  Nivolumab, In Combination With Fluoropyrimidine- And Platinum-Containing Chemotherapy, Is Indicated For The Treatment Of  Patients With Advanced Or Metastatic Gastric Cancer, Gastroesophageal Junction Cancer, And Esophageal Adenocarcinoma.,Adjuvant Treatment Of Resected Esophageal Or Gastroesophageal Junction Cancer (Ec Or Gejc):  Nivolumab Is Indicated For The Adjuvant Treatment Of Completely Resected Esophageal Or Gastroesophageal Junction Cancer With Residual Pathologic Disease In Patients Who Have Received Neoadjuvant Chemoradiotherapy (Crt).","dt_closure_dt":"02-NOV-2022","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Nivolumab 107.0000 Milligram (Mg),Sodium Citrate,Dihydrate 62.9000 Milligram (Mg),Sodium Chloride 31.2000 Milligram (Mg),Mannitol 321.0000 Milligram (Mg),Pentetic Acid 0.0850 Milligram (Mg),Polysorbate 80 2.1400 Milligram (Mg),Hydrochloric Acid 0.0000 Q.S To Ph 6.0,Sodium Hydroxide 0.0000 Q.S To Ph 6.0,Water For Injection 0.0000 Q.S To 10.7 Ml","str_indication":"Nivolumab, In Combination With Platinum-Doublet Chemotherapy, Is Indicated As Neoadjuvant Treatment Of Adult Patients With Resectable (Tumors ?4 Cm Or Node Positive) Non-Small Cell Lung Cancer (Nsclc).","dt_closure_dt":"27-MAY-2024","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Nivolumab 47.0000 Milligram (Mg),Sodium Citrate, Dihydrate 27.6000 Milligram (Mg),Sodium Chloride 13.7000 Milligram (Mg),Mannitol 141.0000 Milligram (Mg),Pentetic Acid 0.0370 Milligram (Mg),Polysorbate 80 0.9400 Milligram (Mg),Hydrochloric Acid 0.0000 Q.S To Ph 6.0,Sodium Hydroxide 0.0000 Q.S To Ph 6.0,Water For Injection 0.0000 Q.S To 4.7 Ml","str_indication":"Nivolumab, In Combination With Platinum-Doublet Chemotherapy, Is Indicated As Neoadjuvant Treatment Of Adult Patients With Resectable (Tumors ?4 Cm Or Node Positive) Non-Small Cell Lung Cancer (Nsclc).","dt_closure_dt":"27-MAY-2024","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Nivolumab 250.0000 Milligram (Mg),Sodium Citrate, Dihydrate 147.0000 Milligram (Mg),Sodium Chloride 73.0000 Milligram (Mg),Mannitol 750.0000 Milligram (Mg),Pentetic Acid 0.2000 Milligram (Mg),Polysorbate 80 5.0000 Milligram (Mg),Hydrochloric Acid 0.0000 Q.S To Ph 6.0,Sodium Hydroxide 0.0000 Q.S To Ph 6.0,Water For Injection 0.0000 Q.S To 25.0 Ml","str_indication":"Nivolumab, In Combination With Platinum-Doublet Chemotherapy, Is Indicated As Neoadjuvant Treatment Of Adult Patients With Resectable (Tumors ?4 Cm Or Node Positive) Non-Small Cell Lung Cancer (Nsclc).","dt_closure_dt":"27-MAY-2024","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Nivolumab 10.0000 Mg/Ml","str_indication":"Metastatic Non-Small Cell Lung Cancer,Adjuvant Treatment Of Melanoma,Neoadjuvant Treatment Of Resectable Non-Small Cell Lung Cancer,Malignant Pleural Mesothelioma,Unresectable Or Metastatic Melanoma,Advanced Renal Cell Carcinoma,Classical Hodgkin Lymphoma,Squamous Cell Carcinoma Of The Head And Neck,Urothelial Carcinoma,Adjuvant Treatment Of Urothelial Carcinoma,Microsatellite Instability-High Or Mismatch Repair Deficient Metastatic Colorectal Cancer,Hepatocellular Carcinoma,Oesophageal Squamous Cell Carcinoma,Adjuvant Treatment Of Oesophageal Or Gastro-Oesophageal Junction Cancer,Gastric Cancer, Gastroesophageal Junction Cancer, And Oesophageal Adenocarcinoma","dt_closure_dt":"30-DEC-2024","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Nivolumab","str_composition":"Nivolumab 10.0000 Mg/Ml","str_indication":"Gastric Cancer, Gastroesophageal Junction Cancer, And Oesophageal Adenocarcinoma,Metastatic Non-Small Cell Lung Cancer,Adjuvant Treatment Of Melanoma,Neoadjuvant Treatment Of Resectable Non-Small Cell Lung Cancer,Malignant Pleural Mesothelioma,Unresectable Or Metastatic Melanoma,Advanced Renal Cell Carcinoma,Classical Hodgkin Lymphoma,Squamous Cell Carcinoma Of The Head And Neck,Urothelial Carcinoma,Adjuvant Treatment Of Urothelial Carcinoma,Microsatellite Instability-High Or Mismatch Repair Deficient Metastatic Colorectal Cancer,Hepatocellular Carcinoma,Oesophageal Squamous Cell Carcinoma,Adjuvant Treatment Of Oesophageal Or Gastro-Oesophageal Junction Cancer","dt_closure_dt":"30-DEC-2024","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Nivolumab","str_composition":"Water For Injection 0.0000 Q.S. To 4.7 Ml,Sodium Citrate, Dihydrate 27.6000 Milligram (Mg),Hydrochloric Acid 0.0000 Q.S. To Ph 6.0,Nivolumab (Bms-936558) 47.0000 Milligram (Mg),Sodium Hydroxide 0.0000 Q.S. To Ph 6.0,Mannitol 141.0000 Milligram (Mg),Nitrogen 0.0000 Not Applicable (Na),Sodium Chloride 13.7000 Milligram (Mg),Pentetic Acid 0.0376 Milligram (Mg),Polysorbate 80 0.9400 Milligram (Mg)","str_indication":"Urothelial Carcinoma (Uc) Nivolumab Is Indicated For The Adjuvant Treatment Of Adult Patients With Urothelial Carcinoma (Uc) Who Are At High Risk Of Recurrence After Undergoing Radical Resection Of Uc.,Esophageal Squamous Cell Carcinoma (Escc)-Nivolumab, In Combination With Fluoropyrimidine- And Platinum-Containing Chemotherapy, Is Indicated For The First-Line Treatment Of Adult Patients With Unresectable Advanced Or Metastatic Esophageal Squamous Cell Carcinoma (Escc),Nivolumab , In Combination With Ipilimumab, Is Indicated For The First-Line Treatment Of Adult Patients With Unresectable Advanced Or Metastatic Esophageal Squamous Cell Carcinoma (Escc)","dt_closure_dt":"19-JAN-2024","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"NA","str_indication":"NA","dt_closure_dt":"30-DEC-2024","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Nivolumab","str_composition":"Hydrochloric Acid 0.0000 Q.S. To Ph 6.0,Sodium Chloride 31.2000 Milligram (Mg),Each Vial Includes A 0.7 Ml Overfill For Vial, Needle, And Syringe (Vns) Holdup 0.7000 Ml,Sodium Hydroxide 0.0000 Q.S. To Ph 6.0,Pentetic Acid 0.0850 Milligram (Mg),Water For Injection 0.0000 Q.S. To 10.7 Ml,Polysorbate 80 2.1400 Milligram (Mg),Mannitol 321.0000 Milligram (Mg),Sodium Citrate, Dihydrate 62.9000 Milligram (Mg),Nivolumab 107.0000 Milligram (Mg)","str_indication":"Nivolumab Is Indicated For The Adjuvant Treatment Of Completely Resected Esophageal Or Gastroesophageal Junction Cancer With Residual Pathologic Disease In Patients , Who Have Received Neoadjuvant Chemoradiotherapy (Crt).,Nivolumab, In Combination With Fluoropyrimidine- And Platinum-Containing Chemotherapy, Is Indicated For The Treatment Of Patients With Advanced Or Metastatic Gastric Cancer, Gastroesophageal Junction Cancer, And Esophageal Adenocarcinoma.","dt_closure_dt":"30-NOV-2021","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Sodium Citrate, Dihydrate 62.9000 Milligram (Mg),Sodium Hydroxide 0.0000 Q.S. To Ph 6.0,Pentetic Acid 0.0850 Milligram (Mg),Polysorbate 80 2.1400 Milligram (Mg),Nitrogen 0.0000 Not Applicable (Na),Sodium Chloride 31.2000 Milligram (Mg),Water For Injection 0.0000 Q.S. To 10.7 Ml,Nivolumab (Bms-936558) 107.0000 Milligram (Mg),Hydrochloric Acid 0.0000 Q.S. To Ph 6.0,Mannitol 321.0000 Milligram (Mg)","str_indication":"Urothelial Carcinoma (Uc) Nivolumab Is Indicated For The Adjuvant Treatment Of Adult Patients With Urothelial Carcinoma (Uc) Who Are At High Risk Of Recurrence After Undergoing Radical Resection Of Uc.,Esophageal Squamous Cell Carcinoma (Escc)-Nivolumab, In Combination With Fluoropyrimidine- And Platinum-Containing Chemotherapy, Is Indicated For The First-Line Treatment Of Adult Patients With Unresectable Advanced Or Metastatic Esophageal Squamous Cell Carcinoma (Escc),Nivolumab , In Combination With Ipilimumab, Is Indicated For The First-Line Treatment Of Adult Patients With Unresectable Advanced Or Metastatic Esophageal Squamous Cell Carcinoma (Escc)","dt_closure_dt":"19-JAN-2024","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Nivolumab 47.0000 Milligram (Mg),Sodium Citrate, Dihydrate 27.6000 Milligram (Mg),Sodium Chloride 13.7000 Milligram (Mg),Mannitol 141.0000 Milligram (Mg),Pentetic Acid 0.0370 Milligram (Mg),Polysorbate 80 0.9400 Milligram (Mg),Hydrochloric Acid 0.0000 Q.S To Ph 6.0,Water For Injection 0.0000 Q.S To 4.7 Ml,Sodium Hydroxide 0.0000 Q.S To Ph 6.0","str_indication":"Renal Cell Carcinoma (Rcc)- Nivolumab, In Combination With Cabozantinib, Is Indicated For The First-Line Treatment Of Patients With Advanced Renal Cell Carcinoma (Rcc).","dt_closure_dt":"04-SEP-2023","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Nivolumab 107.0000 Milligram (Mg),Sodium Citrate, Dihydrate 62.9000 Milligram (Mg),Sodium Chloride 31.2000 Milligram (Mg),Mannitol 321.0000 Milligram (Mg),Pentetic Acid 0.0850 Milligram (Mg),Polysorbate 80 2.1400 Milligram (Mg),Sodium Hydroxide 0.0000 0.0 Q.S To Ph 6.0,Hydrochloric Acid 0.0000 Q.S To Ph 6.0,Water For Injection 0.0000 Q.S To 10.7 Ml","str_indication":"Renal Cell Carcinoma (Rcc)- Nivolumab, In Combination With Cabozantinib, Is Indicated For The First-Line Treatment Of Patients With Advanced Renal Cell Carcinoma (Rcc).","dt_closure_dt":"04-SEP-2023","str_man_unit_name":"Bristol-Myers Squibb India Pvt. Ltd."},{"str_drug_name":"Nivolumab","str_composition":"Nivolumab 47.0000 Milligram (Mg),Sodium Citrate, Dihydrate 27.6000 Milligram (Mg),Sodium Chloride 13.7000 Milligram (Mg),Mannitol 141.0000 Milligram (Mg),Pentetic Acid 0.0370 Milligram (Mg),Polysorbate 80 0.9400 Milligram (Mg),Hydrochloric Acid 0.0000 Q.S To Ph 6.0,Sodium Hydroxide 0.0000 Q.S To Ph 6.0,Water For Injection 0.0000 Q.S. To 4.7 Ml,Each Vial Includes A 0.7 Ml Overfill For Vial, Needle, And Syringe (Vns) Holdup. 0.7000 Ml","str_indication":"Nivolumab Is Indicated For The Treatment Of Patients With Unresectable Advanced, Recurrent, Or Metastatic Esophageal Squamous Cell Carcinoma (Escc) After Prior Fluoropyrimidine- And Platinum-Based Chemotherapy.","dt_closure_dt":"04-AUG-2021","str_man_unit_name":"Bristol-Myers Squibb India Pvt. 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Prior therapy should have included an anthracycline unless clinically contraindicated.","dt_closure_dt":"22.01.14","str_man_unit_name":""},{"str_drug_name":"Paclitaxel Lipid Suspension For Injection 100 Mg/Vial","str_composition":"Paclitaxel 100.0000 Milligram (Mg),Soy Phosphatidyl Choline 3971.5000 Milligram (Mg),Sodium Cholesteryl Sulfate 28.5000 Milligram (Mg),Monosodium Citrate 200.0000 Milligram (Mg),Peg 400 1500.0000 Milligram (Mg),Sucrose 15000.0000 Milligram (Mg)","str_indication":"For The Treatment Of Breast Cancer After Failure Of Combination Chemotherapy For Metastatic Disease Or Relapse Within 6 Months Of Adjuvant Chemotherapy. Prior Therapy Should Have Included An Anthracycline Unless Clinically Contraindicated.,For The Adjuvant Treatment Of Node- Positive Breast Cancer Administered Sequentially To Standard Doxorubicin-Containing Combination Chemotherapy.,As A First-Line And Subsequent Therapy For The Treatment Of Advanced Carcinoma Of The Ovary. 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(?g)","str_indication":"Treatment For Sars Cov 02 (Covid 19)","dt_closure_dt":"23-APR-2021","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Pegylated Interferon Alfa-2b, Pegifn Aplha 2b, Pegylated Interferon Alfa-2b, , Pegylated Interferon Alfa-2b, , Pegylated Interferon Alfa-2b, , Pegylated Interferon Alfa-2b, ","str_composition":"NA","str_indication":"NA","dt_closure_dt":"23-APR-2021","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Pegylated liposomal doxorubicin hcl inj.","str_composition":"","str_indication":"Additional indication- metastatic breast cancer in patients where there is an increased cardial risk.","dt_closure_dt":"14-05-2003","str_man_unit_name":"Fulford"},{"str_drug_name":"Pegylated Liposomal Irinotecan 4.3 Mg/Ml Concentrate For Solution For Infusion","str_composition":"Irinotecan Anhydrous Free Base 4.3000 Mg/Ml","str_indication":"For The Treatment Of Metastatic Adenocarcinoma Of The Pancreas, In Combination With 5-Fluorouracil (5-Fu) And Leucovorin (Lv), In Adult Patients Who Have Progressed Following Gemcitabine-Based Therapy","dt_closure_dt":"01-NOV-2021","str_man_unit_name":"SERVIER INDIA PRIVATE LIMITED"},{"str_drug_name":"Pegylated Recombinant Methionyl Human Granulocyte Colony Stimulating Factor (Peg-R-Met-Hu-G-Csf)","str_composition":"Pegfilgrastim 6.0000 Mg/0.6ml,Acetate 0.5900 Mg/Ml,Polysorbate 20 0.0030 % W/V,D-Sorbitol 5.0000 % W/V,Sodium Hydroxide 0.1000 Ml To Q.S.,Water For Injection 0.6000 Ml To Q.S.","str_indication":"Reduction In The Duration Of Neutropenia And The Incidence Of Febrile Neutropenia In Patients Treated With Cytotoxic Chemotherapy For Malignancy","dt_closure_dt":"19-SEP-2024","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Pembrolizumab Injection 100mg/4ml","str_composition":"Pembrolizumab 100.0000 Mg/4ml","str_indication":"Pembrolizumab As Monotherapy Is Indicated For The Adjuvant Treatment Of Adults With Non-Small Cell Lung Carcinoma Who Are At High Risk Of Recurrence Following Complete Resection And Platinum-Based Chemotherapy.,Pembrolizumab In Combination With Platinum-Containing Chemotherapy As Neoadjuvant Treatment, And Then Continued As Monotherapy As Adjuvant Treatment, Is Indicated For The Treatment Of Resectable Non Small Cell Lung Carcinoma At High Risk Of Recurrence In Adults.,Pembrolizumab, In Combination With Trastuzumab, Fluoropyrimidine And Platinum-Containing Chemotherapy, Is Indicated For The First-Line Treatment Of Locally Advanced Unresectable Or Metastatic Her2-Positive Gastric Or Gastro-Oesophageal Junction Adenocarcinoma In Adults Whose Tumours Express Pd-L1 With A Cps ? 1.,Pembrolizumab, In Combination With Fluoropyrimidine And Platinum-Containing Chemotherapy, Is Indicated For The First-Line Treatment Of Locally Advanced Unresectable Or Metastatic Her2-Negative Gastric Or Gastro-Oesophageal Junction Adenocarcinoma In Adults Whose Tumours Express Pd-L1 With A Cps ? 1.,Pembrolizumab, In Combination With Gemcitabine And Cisplatin, Is Indicated For The First-Line Treatment Of Locally Advanced Unresectable Or Metastatic Biliary Tract Carcinoma In Adults.","dt_closure_dt":"22-APR-2025","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Pembrolizumab Injection 100mg/4ml","str_composition":"Pembrolizumab 100.0000 Mg/4ml","str_indication":"Pembrolizumab As Monotherapy Is Indicated For The Adjuvant Treatment Of Adults With Stage Iii Melanoma And Lymph Node Involvement Who Have Undergone Complete Resection.,Pembrolizumab As Monotherapy Is Indicated For The First-Line Treatment Of Metastatic Microsatellite Instability-High (Msi-H) Or Mismatch Repair Deficient (Dmmr) Colorectal Cancer In Adults.,Pembrolizumab As Monotherapy Is Indicated For The Treatment Of Adult With Relapsed Or Refractory Classical Hodgkin Lymphoma Who Have Failed Autologous Stem Cell Transplant (Asct) Or Following At Least Two Prior Therapies When Asct Is Not A Treatment Option.","dt_closure_dt":"06-MAR-2024","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Pembrolizumab Injection 100mg/4ml","str_composition":"Pembrolizumab 100.0000 Mg/4ml","str_indication":"Pembrolizumab, In Combination With Chemoradiotherapy (External Beam Radiation Therapy Followed By Brachytherapy), Is Indicated For The Treatment Of Figo 2014 Stage Iii - Iva Locally Advanced Cervical Cancer In Adults Who Have Not Received Prior Definitive Therapy.,Pembrolizumab, In Combination With Fluoropyrimidine And Platinum-Containing Chemotherapy, Is Indicated For The First-Line Treatment Of Locally Advanced Unresectable Or Metastatic Her2-Negative Gastric Or Gastro-Oesophageal Junction Adenocarcinoma In Adults Whose Tumours Express Pd L1 With A Cps ? 1.,Pembrolizumab, In Combination With Gemcitabine And Cisplatin, Is Indicated For The First-Line Treatment Of Locally Advanced Unresectable Or Metastatic Biliary Tract Carcinoma In Adults.","dt_closure_dt":"19-NOV-2025","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Pembrolizumab Injection 100mg/4ml (25mg/Ml In A Single Vial)","str_composition":"Pembrolizumab 100.0000 Mg/4ml","str_indication":"Renal Cell Carcinoma (Rcc) - Pembrolizumab, In Combination With Axitinib, Is Indicated For The First-Line Treatment Of Advanced Renal Cell Carcinoma In Adults. Pembrolizumab As Monotherapy Is Indicated For The Adjuvant Treatment Of Adults With Renal Cell Carcinoma At Increased Risk Of Recurrence Following Nephrectomy Or Following Nephrectomy And Resection Of Metastatic Lesions (For Selection Criteria, See Clinical Studies),Triple-Negative Breast Cancer (Tnbc) - Pembrolizumab, In Combination With Chemotherapy As Neoadjuvant Treatment, And Then Continued As Monotherapy As Adjuvant Treatment After Surgery, Is Indicated For The Treatment Of Adults With Locally Advanced, Or Early-Stage Triple-Negative Breast Cancer At High Risk Of Recurrence. Pembrolizumab, In Combination With Chemotherapy, Is Indicated For The Treatment Of Locally Recurrent Unresectable Or Metastatic Triple-Negative Breast Cancer In Adults Whose Tumours Express Pd-L1 With A Cps ? 10 And Who Have Not Received Prior Chemotherapy For Metastatic Disease.","dt_closure_dt":"01-JUN-2023","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Pembrolizumab Injection 100mg/4ml (25mg/Ml In A Single Vial)","str_composition":"Pembrolizumab 100.0000 Mg/4ml","str_indication":"Cervical Cancer - Pembrolizumab, In Combination With Chemotherapy With Or Without Bevacizumab, Is Indicated For The Treatment Of Patients With Persistent, Recurrent, Or Metastatic Cervical Cancer.,Esophageal Cancer - Pembrolizumab, In Combination With Platinum- And Fluoropyrimidine-Based Chemotherapy, Is Indicated For The First-Line Treatment Of Patients With Locally Advanced Unresectable Or Metastatic Carcinoma Of The Esophagus Or Gastroesophageal Junction.","dt_closure_dt":"25-NOV-2022","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Pemetrexed Disodium 500mg/100mg Powder for Injection","str_composition":"","str_indication":"As monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has to progressed immediately following platinum based chemotherapy.","dt_closure_dt":"30.10.12","str_man_unit_name":""},{"str_drug_name":"Pemetrexed Disodium 500mg/100mg Powder for Injection (additional indication)","str_composition":"","str_indication":"Indicated as a monotherapy for the maintenance treatment of locally advanced or metastatic Non Small Cell Lung Cancer (NSCLC) other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-baseޡ\u0005","dt_closure_dt":"16.01.10","str_man_unit_name":""},{"str_drug_name":"Pemetrexed disodium 500mg/100mg powder for sol. (Addl.indication )","str_composition":"","str_indication":"In combination with cisplatin is indicated for the first line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.","dt_closure_dt":"08.10.08","str_man_unit_name":""},{"str_drug_name":"Pemetrexed disodium 500mg / 100mg powder for sol. (Addl. Indication)","str_composition":"","str_indication":"As monotherapy for the second-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.","dt_closure_dt":"04.12.08","str_man_unit_name":""},{"str_drug_name":"Pemetrexed Disodium Injection 10 Mg/Ml (10 Ml, 50 Ml, 85 Ml And 100 Ml Fills )","str_composition":"Pemetrexed Disodium 10.0000 Mg/Ml","str_indication":"Pemetrexed In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer Other Than Predominantly Squamous Cell Histology,Pemetrexed Is Indicated As Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy,Pemetrexed Is Indicated As Monotherapy For The Second Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer Other Than Predominantly Squamous Cell Histology","dt_closure_dt":"28-JUL-2023","str_man_unit_name":"Shilpa Medicare Limited, Unit-IV"},{"str_drug_name":"Pemetrexed For Injection","str_composition":"Pemetrexed Disodium 500.0000 Milligram (Mg)","str_indication":"In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Nsclc, With No Egfr Or Alk Genomic Tumor Aberrations.","dt_closure_dt":"08-MAR-2021","str_man_unit_name":"Reliance Life Sciences Pvt Ltd "},{"str_drug_name":"Pemetrexed For Injection","str_composition":"Pemetrexed Disodium 100.0000 Milligram (Mg)","str_indication":"In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Nsclc, With No Egfr Or Alk Genomic Tumor Aberrations.","dt_closure_dt":"08-MAR-2021","str_man_unit_name":"Reliance Life Sciences Pvt Ltd "},{"str_drug_name":"Pemetrexed For Injection 1000 Mg (Lyophilized)","str_composition":"Pemetrexed Disodium Heptahydrate 1000.0000 Milligram (Mg)","str_indication":"Indicated As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy. First Line Treatment Should Be A Platinum Doublet With Gemcitabine, Paclitaxel Or Docetaxel.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer Other Than Predominantly Squamous Cell Histology,As Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer Other Than Predominantly Squamous Cell Histology,As Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has To Progressed Immediately Following Platinum Based Chemotherapy.","dt_closure_dt":"16-JUL-2021","str_man_unit_name":"BDR Pharmaceuticals International Pvt Ltd"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To Pemetrexed 7.0000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy.,In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To Pemetrexed 9.0000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy.,In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To Pemetrexed 8.5000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy.,In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To Pemetrexed 10.0000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy.,In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To Pemetrexed 11.0000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy.,In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To Pemetrexed 7.5000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy.,In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To Pemetrexed 6.0000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy.,In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To  Pemetrexed 5.0000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy.,In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To Pemetrexed 6.5000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Second-Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology.,As A Monotherapy For The Maintenance Treatment Of Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than Predominantly Squamous Cell Histology In Patients Whose Disease Has Not Progressed Immediately Following Platinum-Based Chemotherapy.,In Combination With Pembrolizumab And Platinum Chemotherapy, For The Initial Treatment Of Patients With Metastatic Non-Squamous Non-Small Cell Lung Cancer (Nsclc), With No Egfr Or Alk Genomic Tumor Aberrations","dt_closure_dt":"03-SEP-2021","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Pemetrexed Solution For Infusion (5 Mg/Ml, 6 Mg/Ml, 6.5 Mg/Ml, 7 Mg/Ml, 7.5 Mg/Ml, 8 Mg/Ml, 8.5 Mg/Ml, 9 Mg/Ml, 10 Mg/Ml And 11 Mg/Ml), 100 Ml Ready To Use Infusion Bag","str_composition":"Pemetrexed Disodium Heptahydrate Ip Equivalent To Pemetrexed 8.0000 Milligram (Mg)","str_indication":"In Combination With Cisplatin For The Treatment Of Chemotherapy Naive Patients With Unresectable Malignant Pleural Mesothelioma.,In Combination With Cisplatin Is Indicated For The First Line Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Other Than 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For The Treatment Of Invasive Aspergillosis.","dt_closure_dt":"26-APR-2022","str_man_unit_name":"Glenmark Pharmaceuticals Ltd."},{"str_drug_name":"Posaconazole","str_composition":"Posaconazole 95.0000 %,Propylgallate 60.0000 %,Unspecified Impurity 0.2000 %,Total Impurity 2.0000 %","str_indication":"To Treat Fungal Infections","dt_closure_dt":"15-FEB-2021","str_man_unit_name":"AET LABORATORIES PRIVATE LIMITED"},{"str_drug_name":"Posaconazole 100 Mg Gastro-Resistant Tablets","str_composition":"Posaconazole 100.0000 Milligram (Mg)","str_indication":"Posaconazole Gastro Resistant Tablets Are Indicated For The Treatment Of Oropharyngeal Candidiasis, Including Oropharyngeal Candidiasis Refractory To Itraconazole And/Or Fluconazole. For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients, 13 Years Of Age And Older, Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus-Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy. Zygomycosis (Mucormycosis) In Patients With Disease Refractory To Other Therapy, Or Patients Who Are Intolerant Other Therapy.","dt_closure_dt":"30-JUL-2021","str_man_unit_name":"AET LABORATORIES PRIVATE LIMITED"},{"str_drug_name":"Posaconazole 300mg Gastro-Resistant Tablets","str_composition":"Posaconazole 300.0000 Milligram (Mg)","str_indication":"Posaconazole Gastro Resistant Tablets Are Indicated For The Treatment Of Oropharyngeal Candidiasis,  Including Oropharyngeal Candidiasis Refractory To Itraconazole And/Or Fluconazole.  For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients, 13 Years Of Age And Older,  Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As  Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus-Host Disease (Gvhd) Or Those  With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy. Zygomycosis (Mucormycosis) In Patients With Disease Refractory To Other Therapy, Or Patients Who Are  Intolerant Other Therapy.","dt_closure_dt":"17-AUG-2021","str_man_unit_name":"AET LABORATORIES PRIVATE LIMITED"},{"str_drug_name":"Posaconazole Delayed Release Tablet 100mg","str_composition":"Posaconazole 100.0000 Milligram (Mg)","str_indication":"For The Treatment Of Oropharyngeal Candidiasis, Including Oropharyngeal Candidiasis Refractory To Itraconazole And/Or Fluconazole.,For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients, 13 Years Of Age And Older, Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus�-Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy.,Zygomycosis (Mucormycosis) In Patients With Disease Refractory To Other Therapy, Or Patients Who Are Intolerant Of Other Therapy.","dt_closure_dt":"21-FEB-2022","str_man_unit_name":"MSD Pharmaceutical Private Limited"},{"str_drug_name":"Posaconazole Delayed Release Tablets 100mg","str_composition":"Posaconazole 100.0000 Milligram (Mg)","str_indication":"Posaconazole Delayed Release Tablets Are Indicated For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised Such As Hematopoietic Stem Cell Transplant Hsct Recipients With Graft Versus Host Disease Gvhd Or Those With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy Posaconazole Delayed Release Tablets Are Indicated In Patients 13 Years Of Age And Older","dt_closure_dt":"24-FEB-2020","str_man_unit_name":"Hetero Labs Limited"},{"str_drug_name":"Posaconazole Delayed Release Tablets 100 Mg","str_composition":"Posaconazole 100.0000 Milligram (Mg),Microcrystalline Cellulose (Flocel101bd) 150.0000 Milligram (Mg),Hpmc As(Aqoat As-Mg) 100.0000 Milligram (Mg),Eudragit L100 120.0000 Milligram (Mg),Microcrystalline Cellulose (Flocel 102) 40.0000 Milligram (Mg),Croscarmellose Sodium 25.0000 Milligram (Mg),Colloidal Anhydrous Silica 3.0000 Milligram (Mg),Magnesium Stearate 6.0000 Milligram (Mg),Opadry Ii 85f520271 Yellow 16.0000 Milligram (Mg)","str_indication":"It Is Indicated For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus-Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy.","dt_closure_dt":"10-JUN-2021","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Posaconazole Delayed-Release Tablets 100 Mg","str_composition":"Posaconazole 100.0000 Milligram (Mg)","str_indication":"Posaconazole Delayed-Release Tablets Is Indicated For Use In The Treatment Of The Following Fungal Infections In Patients 13 Years Of Age And Older:   \t Invasive Aspergillosis In Patients With Disease That Is Refractory To Amphotericin B Or Itraconazole Or In Patients Who Are Intolerant Of These Medicinal Products; \tFusariosis In Patients With Disease That Is Refractory To Amphotericin B Or In Patients Who Are Intolerant Of Amphotericin B; \tChromoblastomycosis And Mycetoma In Patients With Disease That Is Refractory To Itraconazole Or In Patients Who Are Intolerant Of Itraconazole; \tCoccidioidomycosis In Patients With Disease That Is Refractory To Amphotericin B, Itraconazole Or Fluconazole Or In Patients Who Are Intolerant Of These Medicinal Products; \tZygomycosis In Patients With Disease Refractory To Other Therapy, Or Patients Who Are Intolerant Of Other Therapy.,Refractoriness Is Defined As Progression Of Infection Or Failure To Improve After A Minimum Of 7 Days Of Prior Therapeutic Doses Of Effective Antifungal Therapy.     Posaconazole Delayed-Release Tablets Is Also Indicated For Prophylaxis Of Invasive Fungal Infections In The Following Patients:   \t Patients Receiving Remission-Induction Chemotherapy For Acute Myelogenous Leukemia (Aml) Or Myelodysplastic Syndromes (Mds) Expected To Result In Prolonged Neutropenia And Who Are At High Risk Of Developing Invasive Fungal Infections;  Hematopoietic Stem Cell Transplant (Hsct) Recipients Who Are Undergoing High-Dose Immunosuppressive Therapy For Graft Versus Host Disease And Who Are At High Risk Of Developing Invasive Fungal Infections.","dt_closure_dt":"04-JUN-2021","str_man_unit_name":"Fulford (India) Limited"},{"str_drug_name":"Posaconazole Delayed-Release Tablets 100 Mg","str_composition":"Posaconazole 100.0000 Milligram (Mg)","str_indication":"Posaconazole Delayed-Release Tablets Is Indicated For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus-Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy.  Posaconazole Delayed-Release Tablet Is Indicated In Patients 13 Years Of Age And Older.","dt_closure_dt":"14-SEP-2020","str_man_unit_name":"Fulford (India) Limited"},{"str_drug_name":"Posaconazole Gastro-Resistant Tablet","str_composition":"Posaconazole 100.0000 Milligram (Mg)","str_indication":"Posasign Gastro-Resistant Tablets Are Indicated For Use In The Treatment Of Fungal Infections In Adults","dt_closure_dt":"12-SEP-2022","str_man_unit_name":"SIGNATURE PHYTOCHEMICAL INDUSTRIES"},{"str_drug_name":"Posaconazole Gastro-Resistant Tablet 100 Mg","str_composition":"Posaconazole 100.0000 %","str_indication":"For Prophylaxis Of Invasive Aspregilus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus-Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia Form Chemotherapy. Posaconazole Gastro Resistant Tablets Are Indicated In Patients 13 Years Of Age And Older","dt_closure_dt":"03-JAN-2022","str_man_unit_name":"SAVI HEALTH SCIENCE"},{"str_drug_name":"Posaconazole Gastro Resistant Tablets","str_composition":"Posaconazole 300.0000 Milligram (Mg)","str_indication":"For The Treatment Of Oropharyngeal Candidiasis, Including Oropharyngeal Candidiasis Refractory To Itraconazole And/Or Fluconazole. For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients, 13 Years Of Age And Older, Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy. Zygomycosis (Mucormycosis). In Patients With Disease Refractory To Other Therapy, Or Patients Who Are Intolerant Of Other Therapy \"Warning: To Be Sold By Retail On The Prescription Of A Medical Specialist Only?","dt_closure_dt":"25-JUL-2022","str_man_unit_name":"Bajaj Healthcare Ltd"},{"str_drug_name":"Posaconazole Gastro-Resistant Tablets 100 Mg","str_composition":"Posaconazole 100.0000 Milligram (Mg)","str_indication":"For Prophylaxis Of Invasive Aspregilus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versushost Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia Form Chemotherapy,Treatment Of Mucormycosis When Other Antifungal Agents Are Considered Ineffective Or Intolerant","dt_closure_dt":"31-MAY-2021","str_man_unit_name":"Dr Reddys Laboratories Limited"},{"str_drug_name":"Posaconazole Gastro-Resistant Tablets 300mg","str_composition":"Posaconazole 300.0000 Milligram (Mg)","str_indication":"For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus-Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy. Posaconazole Gastro Resistant Tablets Are Indicated In Patients 13 Years Of Age And Older","dt_closure_dt":"07-JUN-2021","str_man_unit_name":"AET LABORATORIES PRIVATE LIMITED"},{"str_drug_name":"Posaconazole Gatro-Resistant Tablet 100 Mg","str_composition":"Posaconazole 100.0000 %","str_indication":"For Prophylaxis Of Invasive Aspregilus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versushost Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia Form Chemotherapy. Posaconazole Gastro Resistant Tablets Are Indicated In Patients 13 Years Of Age And Older","dt_closure_dt":"05-AUG-2021","str_man_unit_name":"Bajaj Healthcare Ltd"},{"str_drug_name":"Posaconazole Injection 18mg/Ml (300mg/16.7ml)","str_composition":"Posaconazole 100.0000 %","str_indication":"For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus-Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy.","dt_closure_dt":"07-JUN-2021","str_man_unit_name":"Naprod Life Sciences Pvt.Ltd "},{"str_drug_name":"Posaconazole Injection 300 Mg/16.7 Ml (18mg/Ml)","str_composition":"Posaconazole Injection 300.0000 Mg Per 16 Point 7 Ml","str_indication":"For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients 13 Years Of Age And Older Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised Such As Hematopoietic Stem Cell Transplant Hsct Recipients With Graft Versus Host Disease Gvhd Or Those With Hematologic Malignancies With Prolonged Neutropenia Form Chemotherapy","dt_closure_dt":"20-SEP-2022","str_man_unit_name":"Hetero Labs Limited"},{"str_drug_name":"Posaconazole Injection 300mg/16.7ml (18mg/Ml)","str_composition":"Posaconazole 18.0000 Mg/Ml","str_indication":"For Prophylaxis Of Invasive Aspergillus And Candida Infections In Patients Who Are At High Risk Of Developing These Infections Due To Being Severely Immunocompromised, Such As Hematopoietic Stem Cell Transplant (Hsct) Recipients With Graft-Versus-Host Disease (Gvhd) Or Those With Hematologic Malignancies With Prolonged Neutropenia From Chemotherapy.","dt_closure_dt":"13-JAN-2020","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Posaconazole Oral Suspension 40mg/ml","str_composition":"","str_indication":"For the treatment of oropharyngeal candidiasis, including oropharyngeal candidiasis refractory to itraconazole and/or fluconazole. For prophylaxis of invasive Aspergillus and Candida infections in patients, 13 years of age and older, who are at high risk ޡ\u0005","dt_closure_dt":"18.07.09","str_man_unit_name":""},{"str_drug_name":"Posaconazole oral suspension 40 mg/ml (additional Indication)","str_composition":"","str_indication":"Zygomycosis in patients with disease refractory to other therapy, or patients who are intolerant of other therapy.","dt_closure_dt":"20.12.11","str_man_unit_name":""},{"str_drug_name":"Potassium Bicarbonate+Sodium Alginate","str_composition":"Sodium Alginate Ip 500.0000 Milligram (Mg),Potassium Bicarbonate Bp 100.0000 Milligram (Mg)","str_indication":"Treatment Of Symptoms Resulting From The Reflux Of Acid, Bile And Pepsin Into The Oesophagus Such As Acid Regurgitation,Heartburn, Indigestion (Occurring Due To The Reflux Of Stomach Contents), For Instance, After Gastric Surgery, As A Result Ofhiatus Hernia, During Pregnancy, Accompanying Reflux Oesophagitis, Including Symptoms Of Laryngopharyngeal Refluxsuch As Hoarseness And Other Voice Disorders, Sore Throats And Cough. It Can Also Be Used To Treat The Symptoms Ofgastro-Oesophageal Reflux During Concomitant Treatment With Or Following Withdrawal Of Acid Suppressing Therapy","dt_closure_dt":"26-JUN-2024","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Potassium Hydrogen Carbonate 200 Mg+Sodium Alginate 1000 Mg","str_composition":"Potassium Hydrogen Carbonate 200.0000 Milligram (Mg)","str_indication":"Treatment Of Symptoms Resulting From The Reflux Of Acid, Bile And Pepsin, Into The Oesophagus Such As Acid Regurgitation, Heartburn, Indigestion (Occurring Due To The Reflux Of The Stomach Contents), For Instance After Gastric Surgery, As A Result Of Hiatus Hernia, During Pregnancy, Accompanying Reflux Of Oesophagitis, Including Symptoms Of Laryngopharyngeal Reflux Such As Hoarseness And Other Voice Disorders, Sore Throats And Cough. It Can Also Be Used To Treat The Symptoms Of Gastro-Oesophageal Reflux During Concomitant Treatment With Or Following Withdrawal Of Acid Suppressing Therapy.","dt_closure_dt":"02-NOV-2021","str_man_unit_name":"Naxpar Pharma Pvt. Ltd."},{"str_drug_name":"Potassium Hydrogen Carbonate 200 Mg+Sodium Alginate 1000 Mg","str_composition":"Sodium Alginate 1000.0000 Milligram (Mg)","str_indication":"Treatment Of Symptoms Resulting From The Reflux Of Acid, Bile And Pepsin, Into The Oesophagus Such As Acid Regurgitation, Heartburn, Indigestion (Occurring Due To The Reflux Of The Stomach Contents), For Instance After Gastric Surgery, As A Result Of Hiatus Hernia, During Pregnancy, Accompanying Reflux Of Oesophagitis, Including Symptoms Of Laryngopharyngeal Reflux Such As Hoarseness And Other Voice Disorders, Sore Throats And Cough. It Can Also Be Used To Treat The Symptoms Of Gastro-Oesophageal Reflux During Concomitant Treatment With Or Following Withdrawal Of Acid Suppressing Therapy.","dt_closure_dt":"02-NOV-2021","str_man_unit_name":"Naxpar Pharma Pvt. Ltd."},{"str_drug_name":"Potassium Hydrogen Carbonate Ph. Eur+Sodium Alginate Ip","str_composition":"Sodium Alginate Ip 1000.0000 Milligram (Mg),Potassium Hydrogen Carbonate 200.0000 Milligram (Mg)","str_indication":"To Treat The Symptoms Of Gastro-Oesophageal Reflux During Concomitant Treatment With Or Withdrawal Of Acid Suppressing Therapy.","dt_closure_dt":"25-AUG-2025","str_man_unit_name":"Macleods Pharmaceuticals Ltd."},{"str_drug_name":"Potassium Hydrogen Carbonate+Sodium Alginate","str_composition":"Sodium Alginate 1000.0000 Milligram (Mg),Potassium Hydrogen Carbonate 200.0000 Milligram (Mg)","str_indication":"Treatment Of Symptoms Of Gastro-Oesophageal Reflux Such As Acid Regurgitation, Heart Burn And Indigestion Related To Reflux, For Example Following Meals Or During Pregnancy Or With Or Following The Withdrawal Of Acid Suppressing Therapy.","dt_closure_dt":"25-JUL-2025","str_man_unit_name":"Espi Industries And Chemicals Pvt Ltd"},{"str_drug_name":"Potassium Hydrogen Carbonate+Sodium Alginate","str_composition":"Sodium Alginate Ip 1000.0000 Milligram (Mg),Potassium Hydrogen Carbonate Ep 200.0000 Milligram (Mg)","str_indication":"To Treat The Symptoms Of Gastro-Oesophageal Reflux During Concomitant Treatment With Or Withdrawal Of Acid Suppressing Therapy.","dt_closure_dt":"14-JAN-2025","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Povidone Iodine","str_composition":"i) Betadine solution containing-10% Povidone Iodine, ii)Betadine gargle containing-0.5% of Povidone iodine, iii)Betadine ointment containing-10% Povidone iodine.","str_indication":"","dt_closure_dt":"1972- November","str_man_unit_name":"Chemo pharma Bombaby"},{"str_drug_name":"Povidone Iodine Alcoholic Prep 10% W/V","str_composition":"Ethanol 30.0000 %V/V,Povidone Iodine 10.0000 % W/V","str_indication":"To Be Used For The Disinfection Of The Skin Prior To Invasion Surgical Procedures","dt_closure_dt":"20-JAN-2025","str_man_unit_name":"G.S.Pharmbutor Private Ltd."},{"str_drug_name":"Povidone Iodine Gargle 2 Percent Weight By Volume","str_composition":"Povidone Iodine 2.0000 % W/V","str_indication":"As Oral Antiseptic For Infected Inflammatory Conditions Of The Mouth And Pharynx Such As Tonsillitis, Pharyngitis, Stomatitis, Traumatic Ulcers Etc. And For Maintaining Oral Hygiene Prior To, During And After Dental And Oral Surgery.","dt_closure_dt":"31-AUG-2023","str_man_unit_name":"STEDMAN PHARMACEUTICALS PVT.LTD."},{"str_drug_name":"Povidone Iodine Nasal Solution 0.5% W/V","str_composition":"Povidone Iodine 0.5000 % W/V","str_indication":"Topical Solution For Nasal Use. For Decontamination And Microbial Decolonization Of Nasal Mucosa.","dt_closure_dt":"02-APR-2025","str_man_unit_name":"G.S.Pharmbutor Private Ltd."},{"str_drug_name":"Povidone Iodine Sachet (containing Effervescent Granules) Each 2gm Sachet contains: 175mg (available iodine 17.5mg)","str_composition":"","str_indication":"As mouthwash for oral hygeine in various oropharyngeal conditions, surgery, dental infections, and halitosis.","dt_closure_dt":"25.08.08","str_man_unit_name":""},{"str_drug_name":"Povidone iodine sterile ophthalmic prep solution","str_composition":"Each ml contains; povidone iodine IP-5.0% w/v","str_indication":"For prepping of the periocular region and irrigation of the ocular surfaces.","dt_closure_dt":"22/11/1996","str_man_unit_name":"Milmet labs"},{"str_drug_name":"Povidone Iodine Throat Spray 0.45% W/V","str_composition":"Povidone Iodine 0.4500 % W/V,Ethanol 20.0000 %V/V","str_indication":"Indicated For The Treatment Of Acute Mucosal Infections Of The Mouth And Pharynx Including Stomatitis, Gingivitis, Aphthous Ulcers, Pharyngitis, Tonsillitis, Monilial Infections, Common Colds And Influenza. For Oral Hygiene Prior To, During And After Dental And Oral Surgery. For Fast And Soothing Relief Of Sore Throat","dt_closure_dt":"17-DEC-2024","str_man_unit_name":"G.S.Pharmbutor Private Ltd."},{"str_drug_name":"Povidone Iodine USP","str_composition":"Povidone Iodine USP-4% (Scrub), Povidone Iodine USP-5%(Solution & oitment)","str_indication":"","dt_closure_dt":"1978-September","str_man_unit_name":"Wockhardt, Bombay"},{"str_drug_name":"P-Piperidineethoxy-O-Carbomethoxy Benzophenone Hydrochloride","str_composition":"5mg to 10mg","str_indication":"Antispasmodic and analgesic.","dt_closure_dt":"1961- February","str_man_unit_name":"Hoechst pharm, Bombay"},{"str_drug_name":"Practolol","str_composition":"","str_indication":"Cardiac Drug.","dt_closure_dt":"1973-November","str_man_unit_name":"Cipla, The Alkalic chemical company"},{"str_drug_name":"Practolol ","str_composition":"Each tablet contains; Practolol BP-100mg","str_indication":"","dt_closure_dt":"1974","str_man_unit_name":"Cipla, Bombay"},{"str_drug_name":"Pralidoxime chloride","str_composition":"","str_indication":"Antidote for poisoning.","dt_closure_dt":"1966- March","str_man_unit_name":"Geoffrey, Bombay"},{"str_drug_name":"Pralidoxime iodide","str_composition":"","str_indication":"Antidote for poisoning","dt_closure_dt":"1966- March","str_man_unit_name":"Bayer (India) ltd., Bombay"},{"str_drug_name":"Pralsetinib Capsule 100mg","str_composition":"Print Ink 0.1500 Mg/Capsule,Hypromellose 93.9100 Mg/Capsule,Fd&C Blue #1 (Brilliant Blue Fcf) 0.1700 Mg/Capsule,Microcrystalline Cellulose  (Avicel Ph102) (Intragranular Excipients) 32.7000 Mg/Capsule,Methanol 0.0000 Q.S.,Pregelatinized Starch (Extragranular Excipients) 14.5000 Mg/Capsule,Magnesium Stearate (Extragranular Excipients) 1.8000 Mg/Capsule,Magnesium Stearate (Intragranular Excipients) 1.8000 Mg/Capsule,Hydroxypropyl Methylcellulose 100.0000 Mg/Capsule,Titanium Dioxide 1.9200 Mg/Capsule,Sodium Bicarbonate (Intragranular Excipients) 80.0000 Mg/Capsule,Pralsetinib 100.0000 Mg/Capsule,Citric Acid, Anhydrous (Intragranular Excipients) 32.7000 Mg/Capsule","str_indication":"Non-Small Cell Lung Cancer (Nsclc):- Pralsetinib Is Indicated For The Treatment Of Adult Patients With Rearranged During Transfection (Ret) Fusion-Positive, Locally Advanced Or Metastatic Nsclc. Ret-Mutant Medullary Thryoid Cancer (Mtc):- Pralsetinib Is Indicated For The Treatment Of Adult And Pediatric Patients 12 Years Of Age And Older With Locally Advanced Or Metastatic Ret-Mutant Mtc Who Require Systemic Therapy. Ret-Fusion Positive Thyroid Cancer:- Pralsetinib Is Indicated For The Treatment Of Adult And Pediatric Patients 12 Years Of Age And Older With Locally Advanced Or Metastatic Ret-Fusion Positive Thyroid Cancer Who Require Systemic Therapy And Who Are Radioactive Iodine-Refractory (If Radioactive Iodine Is Appropriate).","dt_closure_dt":"02-JUN-2022","str_man_unit_name":"Roche Products (India) Private Limited"},{"str_drug_name":"Pramipexole Di HCl monohydrate ER Tablet 0.375/0.75/1.5/3/4.5 mg","str_composition":"","str_indication":"For the treatment of the sign and symptoms of idiopathic parkinsons disease.","dt_closure_dt":"13.03.10","str_man_unit_name":""},{"str_drug_name":"Pramipexole Di-hydrochloride Tablet (0.125mg/0.25mg/0.5mg/1mg/1.5mg)","str_composition":"Each tablet contains; pramipexole dihydrochloride monohydrate-0.125mg, 0.25mg, 0.5mg, 1mg, 1.5mg","str_indication":"For the treatment of the signs and symptoms of idiopathic Parkinson�??s disease.","dt_closure_dt":"25/07/2005","str_man_unit_name":"Sun pharma, intas pharma(24-10-05)"},{"str_drug_name":"Prasterone Dhea","str_composition":"Prasterone 0.0000 %","str_indication":"NA","dt_closure_dt":"14-JUN-2022","str_man_unit_name":"B M Chemie"},{"str_drug_name":"Prasugrel (as Hydrochloride) film coated tablet ....5 mg / 10mg. ","str_composition":"Each film coated tablet contains; prasugrel hydrochloride eq.to prasugrel-5mg, 10mg","str_indication":"To reduce the rate of thrombotic cardiovascular (CV) events (including stent thrombosis) in patients with acute coronary syndrome (ACS) who are to be managed with percutaneous coronary intervention (PCI) as  follows:  �?� Patients with unstable angina (UA) ޡ\u0005","dt_closure_dt":"28.05.10","str_man_unit_name":"Eli Lilly, Gurgaon, MSN lab(13.04.10), Ravenbhel(29.04.10), Sun pharma(28.04.10)"},{"str_drug_name":"Pravastatin 40mg tablet (Additional strength)","str_composition":"Each tab contains; Pravastatin sod. phEur. 40mg","str_indication":"As an adjunct to diet to reduce elevated total cholesterol, LDL-C, Apo-B TG levels and to increase HDL-C in patients with primary hypercholesterolaemia and mixed dyslipidaemia.","dt_closure_dt":"09/08/2006","str_man_unit_name":"Torrent pharma"},{"str_drug_name":"Pravastatin tabs","str_composition":"Each uncoated tablet contains; pravastatin sodium-10mg, 20mg, 40mg","str_indication":"By RMP- primary hypercholesterolemia type IIa, IIb and prevention of cardiovascular events in adults only.","dt_closure_dt":"20-12-2000","str_man_unit_name":"Ranbaxy lab"},{"str_drug_name":"Praziquantel tablets","str_composition":"","str_indication":"Neurocysticercosis- In the treatment of infections brought about the larvas of the pork tapeworm in the central nervous system.","dt_closure_dt":"1986-February","str_man_unit_name":"E. Merk, Bombay"},{"str_drug_name":"Praziquantel tablets","str_composition":"Each tablet contains; praziquantel-600mg","str_indication":"Neurocysticercosis- in the treatment of infections brought about by the larvae of pork tapeworm in the CNS.","dt_closure_dt":"1985-August","str_man_unit_name":"E.Merck, Bombay"},{"str_drug_name":"Praziquntel 175mg + Pyrantel 504mg + Febental 525mg Tablets","str_composition":"","str_indication":"For the treatment of mixed infections with roundworms and tapeworms in dogs.","dt_closure_dt":"30.03.10","str_man_unit_name":""},{"str_drug_name":"Prazocin GITs tablets","str_composition":"2.5mg","str_indication":"In additional indication of B.P.H","dt_closure_dt":"14-09-1999","str_man_unit_name":"Pfizer ltd."},{"str_drug_name":"Prazosin hcl (GITS) tablets","str_composition":"","str_indication":"","dt_closure_dt":"21/06/1995","str_man_unit_name":"Pfizer ltd."},{"str_drug_name":"Prazosin hydrochloride","str_composition":"Each tablet contains; prazosin hcl eq.to 1mg,2mg,5mg, (0.5mg for sun pharma-14-11-90)","str_indication":"All grades of essential primary hypertension and all grades of hypertension.","dt_closure_dt":"1990-June","str_man_unit_name":"Pfizer P Ltd, Bombay"},{"str_drug_name":"Prazosin mesylate","str_composition":"","str_indication":"Mild to moderate hypertension only","dt_closure_dt":"11/03/1999","str_man_unit_name":"Sun pharma, cipla"},{"str_drug_name":"Prednicarbate cream","str_composition":"Each gram of cream contains; prednicarbate-2.5mg","str_indication":"Skin diseases where treatment with topical corticosteroid is appropriate.","dt_closure_dt":"06-08-1997 to 06-08-1999","str_man_unit_name":"Hoechst marrion roussel ltd."},{"str_drug_name":"Prednimustine tablets","str_composition":"","str_indication":"Anti cancer drug- Indicated in the treatment of chronic lymphocytic leukaemia, non-hodgkin's lymphoma and breast cancer.","dt_closure_dt":"1986-July","str_man_unit_name":"E. Merk, Bombay"},{"str_drug_name":"Prednisolone","str_composition":"Each retard tablet contains; prednisolone IP-10 mg","str_indication":"","dt_closure_dt":"1971- December","str_man_unit_name":"Hoechst pharmacent, Bombay"},{"str_drug_name":"Prednisolone + Ofloxacin","str_composition":"","str_indication":"","dt_closure_dt":"2003","str_man_unit_name":""},{"str_drug_name":"Prednisolone Sodium Phosphate Orally Disintegrating Tablet 10/15/30mg","str_composition":"","str_indication":"Indicating for condition required Glucocorticoids activity including collagen disease, allergic disease and hypersensitive reaction.","dt_closure_dt":"26.11.09","str_man_unit_name":""},{"str_drug_name":"Prednisolone stearoylglycolate","str_composition":"Each tablet contains; prednisolone stearoylglucolate-6.65mg, ointment- 1.9g, cream & ointment- 1.9 g","str_indication":"","dt_closure_dt":"1971- February","str_man_unit_name":"Mac hales, Bombay"},{"str_drug_name":"Prednisolone stearoylglycolate","str_composition":"","str_indication":"Corticosteroid","dt_closure_dt":"1970- November","str_man_unit_name":"Mac hales, Bombay"},{"str_drug_name":"Pregabalin 150mg/75mg + Methylcobalamin 750mcg + Alpha lipoic acid 100mg + Pyridoxine 3mg + Folic acid 1.5mg capsule","str_composition":"","str_indication":"For the treatment of painful diabetic neuropathy in adults only.","dt_closure_dt":"12.10.10","str_man_unit_name":""},{"str_drug_name":"Pregabalin 75mg/150mg + Methylcobalamin 750mcg capsules (Additional Strength)","str_composition":"","str_indication":"Same as Approved.","dt_closure_dt":"08.05.08","str_man_unit_name":""},{"str_drug_name":"Pregabalin-75mg/150mg + Methylcobalamine 500mcg cap","str_composition":"","str_indication":"For the treatment of adult patients with peripheral neuropathy.","dt_closure_dt":"12.10.07","str_man_unit_name":""},{"str_drug_name":"Pregabalin 75 Mg + Mecobalamin 1500 Mcg + Nortriptyline 10 Mg Film Coated Tablets","str_composition":"Pregabalin 75.0000 Milligram (Mg),Mecobalamin 1500.0000 Micrograms (?g),Nortriptyline 10.0000 Milligram (Mg)","str_indication":"For The Treatment Of Patients With Diabetic Peripheral Neuropathic Pain With Coexistent Vitamin B12 Deficiency.","dt_closure_dt":"13-DEC-2022","str_man_unit_name":"Synokem Pharmaceuticals Ltd"},{"str_drug_name":"Pregabalin Capsule 25/50/100/200mg (addl. Strength)","str_composition":"","str_indication":"Same as approved.","dt_closure_dt":"19/05/2006","str_man_unit_name":""},{"str_drug_name":"Pregabalin capsule (75/150/300 mg)","str_composition":"","str_indication":"For neuropathic pain.","dt_closure_dt":"25/11/2005","str_man_unit_name":""},{"str_drug_name":"Pregabalin capsules (Addl. Indication)","str_composition":"","str_indication":"Management of fibromyalgia syndrome.","dt_closure_dt":"29.04.08","str_man_unit_name":""},{"str_drug_name":"Pregabalin Extended Release Tablets 82.5 Mg And 165 Mg","str_composition":"Sentry Polyox Wsr 303 Leo Nf 345.0000 Milligram (Mg),Kollidon Sr 476.0000 Milligram (Mg),Pregabalin 82.5000 Milligram (Mg),Opadry Ii 85f505194 Blue 23.0000 Milligram (Mg),Magnesium Stearate 8.6300 Milligram (Mg),Mannitol (Pearlitol Sd 200) 214.8700 Milligram (Mg),Glycerol Dibehanate Ep/Nf (Compritol 888) 23.0000 Milligram (Mg)","str_indication":"For Treatment Of Peripheral Neuropathic Pain In Adults","dt_closure_dt":"17-DEC-2019","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Pregabalin Extended Release Tablets 82.5 Mg And 165 Mg","str_composition":"Kollidon Sr 476.0000 Milligram (Mg),Glycerol Dibehanate Ep/Nf (Compritol 888) 23.0000 Milligram (Mg),Pregabalin 165.0000 Milligram (Mg),Mannitol (Pearlitol Sd 200) 132.3700 Milligram (Mg),Opadry Ii 85f570138 Beige 23.0000 Milligram (Mg),Sentry Polyox Wsr 303 Leo Nf 345.0000 Milligram (Mg),Magnesium Stearate 8.6300 Milligram (Mg)","str_indication":"For Treatment Of Peripheral Neuropathic Pain In Adults","dt_closure_dt":"17-DEC-2019","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Pregabalin Gel 8% W/W","str_composition":"Pregabalin 8.0000 %W/W","str_indication":"For The Treatment Of Diabetic Neuropathic Pain","dt_closure_dt":"08-OCT-2024","str_man_unit_name":"Lyka Labs Ltd"},{"str_drug_name":"Pregabalin Oral Solution","str_composition":"Pregabalin 20.0000 Mg/Ml","str_indication":"Indicated For The Treatment Of Neuropathic Pain Associated With Diabetic Peripheral Neuropathy (Dpn) And Fibromyalgia","dt_closure_dt":"06-JUL-2022","str_man_unit_name":"Kingston Aqua Industries Pvt. 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LTD."},{"str_drug_name":"Purified Hpv Serotype 11 Vlp Antigen (Drug Substance)","str_composition":"Hpv 11l1 Protein 40.0000 Micrograms (?g)","str_indication":"NA","dt_closure_dt":"22-APR-2025","str_man_unit_name":"SERUM INSTITUTE OF INDIA PVT. LTD."},{"str_drug_name":"Purified Hpv Serotype 16 Vlp Antigen (Drug Substance)","str_composition":"Hpv 16 L1 Protein 40.0000 Micrograms (?g)","str_indication":"NA","dt_closure_dt":"19-MAR-2025","str_man_unit_name":"SERUM INSTITUTE OF INDIA PVT. LTD."},{"str_drug_name":"Purified Hpv Serotype 18 Vlpantigen (Drug Substance)","str_composition":"Hpv 18 L1 Protein 20.0000 Micrograms (?g)","str_indication":"NA","dt_closure_dt":"22-APR-2025","str_man_unit_name":"SERUM INSTITUTE OF INDIA PVT. LTD."},{"str_drug_name":"Purified Hpv Serotype 6 Vlp Antigen (Drug Substance)","str_composition":"Hpv 6l1 Protein 20.0000 Micrograms (?g)","str_indication":"NA","dt_closure_dt":"22-APR-2025","str_man_unit_name":"SERUM INSTITUTE OF INDIA PVT. LTD."},{"str_drug_name":"Purified Tetanus Toxoid","str_composition":"Purified Tetanus Toxoid 2500.0000 Lf / Ml","str_indication":"NA","dt_closure_dt":"25-JUL-2025","str_man_unit_name":"SERUM INSTITUTE OF INDIA PVT. 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pygeum africanum extract-50mg","str_indication":"Benign prostate hypertrophy","dt_closure_dt":"30-07-2002","str_man_unit_name":"Banna pharmacaps"},{"str_drug_name":"Pyrantel embonate with fabental suspension","str_composition":"Each ml of suspension contains; pyrantel embonate-14.4mg, febental-15mg","str_indication":"For treatment of infestation caused by round worms, ascarids, hook worms, whip worm in puppies & young dogs.","dt_closure_dt":"23-04-2001","str_man_unit_name":"Bayer, India ltd."},{"str_drug_name":"Pyrantel Pamoate USP","str_composition":"","str_indication":"Anthelmitic","dt_closure_dt":"1972-July","str_man_unit_name":"Pfizer"},{"str_drug_name":"Pyrantel tartrate","str_composition":"","str_indication":"In the treatment if ingestation with G.I round worm in sheep, cattle & swine (Broad spectrum anthelmintic)","dt_closure_dt":"1969- April","str_man_unit_name":"Pfizer P Ltd, Bombay"},{"str_drug_name":"Pyrazinamide","str_composition":"","str_indication":"Anti-tuberculosis.","dt_closure_dt":"1964- September","str_man_unit_name":"Pharrmed Pvt ltd, Bombay"},{"str_drug_name":"Pyrazinamide dispersible tabs","str_composition":"Each dispersible tab contains; pyrazinamide-250mg","str_indication":"Short course treatment of tuberculosis in the paediatric age group.","dt_closure_dt":"06/06/1997","str_man_unit_name":"Hindustan ciba geigy"},{"str_drug_name":"Pyridine 3-carboxylic acid hydroxy methylamide + choline bitartrate","str_composition":"Each tablet contains; PCAHM-0.125g, cholie bitartrate-0.125g","str_indication":"","dt_closure_dt":"1971- July","str_man_unit_name":"Ethnor ltd, Bombay"},{"str_drug_name":"Pyridoxine hcl CR tablet","str_composition":"Each C.R tablet contains; pyridoxine hcl-100mg.","str_indication":"Deficiency of vit.B6 caused by usage of oral contraceptive pill/drug induced pyridoxine deficiency.","dt_closure_dt":"07/05/1992","str_man_unit_name":"Modi mundi pharma, New Delhi"},{"str_drug_name":"Pyridoxine HCL IP 3mg + Nicotinamide IP 100mg + Cyanocobalamin IP 15mcg + Folic acid IP 500mcg  + Chromium Picolinate USP 250mcg Tablet","str_composition":"","str_indication":"For Mineral & Vitamins deficiency states in adult patients.","dt_closure_dt":"23.12.10","str_man_unit_name":""},{"str_drug_name":"Pyritinol","str_composition":"","str_indication":"Cerebral stimulant","dt_closure_dt":"1965- April","str_man_unit_name":"Emedia, Bombay"},{"str_drug_name":"Pyrvinium pamoate","str_composition":"","str_indication":"Anthelmintic","dt_closure_dt":"1962- October","str_man_unit_name":"Park Devis Co."},{"str_drug_name":"Quadrivalent Human Papillomavirus (Type 6, 11, 16, 18) Vaccine (Recombinant)","str_composition":"Human Papillomavirus Type 18 L1 Protein 20.0000 Micrograms (?g),Aluminium Hydroxide (As Al+++) 1.2500 Milligram (Mg),Human Papillomavirus Type 6 L1 Protein 20.0000 Micrograms (?g),Human Papillomavirus Type 16 L1 Protein 40.0000 Micrograms (?g),Human Papillomavirus Type 11 L1 Protein 40.0000 Micrograms (?g)","str_indication":"Cervavac Is Indicated In Girls And Women 9 Through 26 Years Of Age For The Prevention Of The Following Diseases Caused By Human Papillomavirus (Hpv) Types, Included In The Vaccine:  ?Cervical, Vulvar, Vaginal, And Anal Cancer Caused By Hpv Types 16 And 18 ?Genital Warts (Condyloma Acuminata) Caused By Hpv Types 6 And 11 And The Following Precancerous Or Dysplastic Lesions Caused By Hpv Types 6, 11, 16, And 18: ?Cervical Intraepithelial Neoplasia (Cin) Grade 2/3 And Cervical Adenocarcinoma In Situ (Ais) ?Cervical Intraepithelial Neoplasia (Cin) Grade 1 ?Vulvar Intraepithelial Neoplasia (Vin) Grade 2 And Grade 3 ?Vaginal Intraepithelial Neoplasia (Vain) Grade 2 And Grade 3 ? 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LTD."},{"str_drug_name":"Quadrivalent Inactivated Influenza Vaccine (Split Virion) I.P","str_composition":"Hemagglutinin A (H1n1) 15.0000 Micrograms (?g),Hemagglutinin A (H3n2) 15.0000 Micrograms (?g),Hemagglutinin B/(Yamagata Lineage) 15.0000 Micrograms (?g),Hemagglutinin B/(Victoria Lineage) 15.0000 Micrograms (?g),Sodium Phosphate Dibasic Anhydrous 3.8300 G/L,Sodium Chloride 6.6000 G/L,Phosphate Buffer Saline 0.0300 M Qs To 0 Point 5 Ml,Formaldehyde 100.0000 Micrograms (?g),Octylphenol Ethoxylate (Triton� X-100) 250.0000 Micrograms (?g),Sodium Phosphate Monobasic Anhydrous 0.4100 G/L","str_indication":"Fluquadri� Is An Inactivated Quadrivalent Influenza Vaccine Indicated For The Prevention Of Influenza Disease Caused By Influenza Types A And B Viruses Contained In The Vaccine. 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(Purified Chick Embryo Cell Culture Rabies Vaccine) [Pcecv-Pm]","str_composition":"Inactivated Rabies Virus (Pitman Moore Strain) Propagated In Chick Embryo Fibroblast Cell Culture And Inactivated By ?-Propiolactone 2.5000 Iu","str_indication":"Active Immunization Against Rabies. 1. For Intramuscular Administration, Use 1 Full Dose (1 Ml) For Pre-& Post Exposure Prophylaxis. 2. For Intradermal Administration, Use 0.1 Ml Per Id Site For Post Exposure Prophylaxis.","dt_closure_dt":"26-DEC-2024","str_man_unit_name":"Zydus Lifesciences Limited"},{"str_drug_name":"Rabies Vaccine, Human I.P. (Purified Chick Embryo Cell Culture Rabies Vaccine) [Pcecv-Pm]","str_composition":"Inactivated Rabies Virus (Pitman Moore Strain) Propagated In Chick Embryo Fibroblast Cell Culture And Inactivated By ?-Propiolactone 2.5000 Iu","str_indication":"Active Immunization Against Rabies. 1. For Intramuscular Administration, Use 1 Full Dose (1 Ml) For Pre & Post Exposure Prophylaxis. 2. 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Veterinarians And Their Assistants, Animal Care Personnel ,Hunters, Doctors, Rabies Laboratory Personnel, Production Personnel, Army Personnel, Forest And Zoo Personnel, Postmen And Children Who Are Exposed To The Risk Of Rabies. 2. 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Ii) Prevention of MI CV death or stroke in high risk diabetes patients.","dt_closure_dt":"02/11/2006","str_man_unit_name":"Astra zeneca"},{"str_drug_name":"Ramipril 5mg + Hydrochlorthiazide 12.5mg tablets (Additional Strength)","str_composition":"","str_indication":"Same as Approved.","dt_closure_dt":"20.02.08","str_man_unit_name":""},{"str_drug_name":"Ramipril (5mg) + Telmisartan (40mg) tablet","str_composition":"","str_indication":"For Hypertension.","dt_closure_dt":"11/05/2005","str_man_unit_name":""},{"str_drug_name":"Ramipril + candesartan cilexatil tabs","str_composition":"Each uncoated bilayered tab contains; ramipril BP-2.5mg,5mg, candesartan cilexatil eq.to candesartan-8mg","str_indication":"By RMP- for mild to moderate essential hypertension and congestive heart failure (CHF)","dt_closure_dt":"2003","str_man_unit_name":"Okasa pharma"},{"str_drug_name":"Ramipril + Hydrochlorthiazide tabs","str_composition":"Each tab contains; ramipril-2.5mg,5mg, Hydrochlorthiazide-12.5mg,25mg","str_indication":"Mild to moderate hypertension in patient (in whom combination therapy is appropriate) who have been stabilized on the individual components given in the same proportion.","dt_closure_dt":"26/08/1996","str_man_unit_name":"Hoechst India ltd."},{"str_drug_name":"Ramipril MR capsule 10mg","str_composition":"","str_indication":"For the treatment of hypertension/ cardiac failure and myocardial infarction.","dt_closure_dt":"30.07.09","str_man_unit_name":""},{"str_drug_name":"Ramipril MR Capsules 2.5/5 mg (Additional Strength)","str_composition":"","str_indication":"Same As Approved ","dt_closure_dt":"03.07.10","str_man_unit_name":""},{"str_drug_name":"Ramipril + S(-) amlodipine tab","str_composition":"Each tab/cap contains; ramipril-2.5mg, S(-) amlodipine besylate eq.to S(-) amlodipine-2.5mg","str_indication":"For treatment of essential hypertension.","dt_closure_dt":"11/02/2003","str_man_unit_name":"Torrent pharma, emcure pharma"},{"str_drug_name":"Ramipril tablets","str_composition":"1.25mg, 2.5mg, 5mg, 10mg","str_indication":"For additional indication; reducing  the risk of myocardial infarction, stroke, cardiovascular death or revascularization, procedures in diabetic patients 55 yrs of age or more with one or more of the following rosk factors, syst. B.P >160mmHg or diastol.ޡ\u0005","dt_closure_dt":"2005","str_man_unit_name":"Aventis pharma"},{"str_drug_name":"Ramipril tablets/capsules","str_composition":"","str_indication":"Additional indication; ","dt_closure_dt":"2004-December","str_man_unit_name":"Aventis pharma"},{"str_drug_name":"Ramosetron Dispersible Tablet 0.1mg","str_composition":"","str_indication":"For the prevention and treatment of gastrointestinal symptoms (nausea and vomitting) associated with ematogenic cancer chemotherapy.","dt_closure_dt":"12.06.10","str_man_unit_name":""},{"str_drug_name":"Ramosetron Hydrochloride Tablets 2.5mcg, 5mcg, 0.1mg & Injecton 0.3mg/2ml ","str_composition":"1) Each tablet contains; ramosetron hydrochloride-2.5mcg, 5mcg, 0.1mg. 2) Each 2ml injection contains; ramosetron hydrochloride-0.3mg","str_indication":"1) Tablets 0.1mg & Injection 0.3mg/2ml-for the prevention and treatment of gastrointestinal symptoms (nausea and vomiting) associated with emetogenic cancer chemotherapy. 2) Tablets 2.5mcg & 5mcg-for the treatment of adult patients with diarrhoea predominޡ\u0005","dt_closure_dt":"12.11.09","str_man_unit_name":"Cadila healthcare ltd., Ahmedabad"},{"str_drug_name":"Ramucirumab","str_composition":"Ramucirumab 10.0000 Mg/Ml,L-Histidine 0.6500 Mg/Ml,L-Histidine Monohydrochloride 1.2200 Mg/Ml,Glycine 9.9800 Mg/Ml,Sodium Chloride 4.3800 Mg/Ml,Polysorbate 80 0.1000 Mg/Ml,Water For Injection 1.0000 Ml","str_indication":"Gastric Cancer -- Cyramza� (Ramucirumab) In Combination With Paclitaxel Is Indicated For The Treatment Of Adult Patients With Advanced Gastric Cancer Or Gastro-Oesophageal Junction Adenocarcinoma With Disease Progression After Prior Platinum And Fluoropyrimidine Chemotherapy. Cyramza� (Ramucirumab) Monotherapy Is Indicated For The Treatment Of Adult Patients With Advanced Gastric Cancer Or Gastro-Oesophageal Junction Adenocarcinoma With Disease Progression After Prior Platinum Or Fluoropyrimidine Chemotherapy, For Whom Treatment In Combination With Paclitaxel Is Not Appropriate.,Colorectal Cancer-- Cyramza� (Ramucirumab), In Combination With Folfiri (Irinotecan, Folinic Acid, And 5-Fluorouracil), Is Indicated For The Treatment Of Adult Patients With Metastatic Colorectal Cancer (Mcrc) With Disease Progression On Or After Prior Therapy With Bevacizumab, Oxaliplatin And A Fluoropyrimidine.,Non-Small Cell Lung Cancer --  Cyramza� (Ramucirumab) In Combination With Erlotinib Is Indicated For The First-Line Treatment Of Adult Patients With Metastatic Non-Small Cell Lung Cancer With Activating Epidermal Growth Factor Receptor (Egfr) Mutations.  Cyramza�(Ramucirumab) , In Combination With Docetaxel, Is Indicated For The Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) With Disease Progression On Or After Platinum-Based Chemotherapy.,Hepatocellular Carcinoma -- Cyramza� (Ramucirumab) Monotherapy Is Indicated For The Treatment Of Adult Patients With Advanced Or Unresectable Hepatocellular Carcinoma Who Have A Serum Alpha Fetoprotein (Afp) Of ? 400 Ng/Ml And Who Have Been Previously Treated With Sorafenib.","dt_closure_dt":"02-NOV-2020","str_man_unit_name":"Eli Lilly And Company"},{"str_drug_name":"Ranibizumab","str_composition":"Ranibizumab 1.6500 Mg/Pfs Of 0.165 Ml Solution,L-Histidine Hcl Monohydrate 0.2740 Pfs Of 0.165 Ml Solution,L-Histidine 0.0530 Mg/Pfs Of 0.165 Ml Solution,L-Histidine Hcl Monohydrate 0.2740 Mg/Pfs Of 0.165 Ml Solution,Trehalose Dihydrate 16.5000 Mg/Pfs Of 0.165 Ml Solution,Polysorbate 20 0.0160 Mg/Pfs Of 0.165 Ml Solution,Water For Injection 0.1650 Up To 0.165 Ml,Nitrogen 0.0000 Q.S.","str_indication":"Ranibizumab Is Indicated In Adults For The Treatment Of Proliferative Diabetic Retinopathy (Pdr).","dt_closure_dt":"04-AUG-2020","str_man_unit_name":"Sandoz Private Limited"},{"str_drug_name":"Ranibizumab","str_composition":"Ranibizumab 10.0000 Mg/Ml,L-Histidine 0.3210 Mg/Ml","str_indication":"Neovascular (Wet) Age-Related Macular Degeneration (Amd),Macular Edema Following Retinal Vein Occlusion (Rvo),Diabetic Retinopathy (Dr),Myopic Choroidal Neovascularization (Mcnv),Diabetic Macular Edema (Dme)","dt_closure_dt":"02-NOV-2021","str_man_unit_name":"LUPIN LIMITED"},{"str_drug_name":"Ranibizumab","str_composition":"Ranibizumab 2.3000 Mg/0.23 Ml,?,?-Trehalose Dihydrate 10.0000 %,L-Histidine 10.0000 Mm,Polysorbate 20 0.0100 %,Water For Injection 0.2300 Ml (Q.S)","str_indication":"Visual Impairment Due To Diabetic Macular Edema (Dme),Iabetic Retinopathy (Dr)  Visual Impairment Due To Myopic Choroidal Neovascularization (Mcnv),Retinopathy Of Prematurity (Rop) With Zone I (Stage 1+, 2+, 3 Or 3+), Zone Ii (Stage 3+) Or Ap-Rop (Aggressive Posterior Rop) Disease,Macular Edema Following Retinal Vein Occlusion (Rvo)","dt_closure_dt":"09-JUL-2024","str_man_unit_name":"Reliance Life Sciences Pvt Ltd "},{"str_drug_name":"Ranibizumab","str_composition":"Ranibizumab 1.3800 Mg/0.23 Ml,?,?-Trehalose Dihydrate 10.0000 %,L-Histidine 10.0000 Mm,Polyorbate 20 0.0100 %,Water For Injection 0.2300 Ml (Q.S)","str_indication":"Macular Edema Following Retinal Vein Occlusion (Rvo),Visual Impairment Due To Diabetic Macular Edema (Dme),Iabetic Retinopathy (Dr)  Visual Impairment Due To Myopic Choroidal Neovascularization (Mcnv),Retinopathy Of Prematurity (Rop) With Zone I (Stage 1+, 2+, 3 Or 3+), Zone Ii (Stage 3+) Or Ap-Rop (Aggressive Posterior Rop) Disease","dt_closure_dt":"09-JUL-2024","str_man_unit_name":"Reliance Life Sciences Pvt Ltd "},{"str_drug_name":"Ranibizumab","str_composition":"Ranibizumab 10.0000 Mg/Ml,?, ?? 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When Already Being Treated With The Free Combination Of Remogliflozin And Teneligliptin","dt_closure_dt":"30-JUN-2021","str_man_unit_name":"Glenmark Pharmaceuticals Ltd."},{"str_drug_name":"Remogliflozin Etabonate+Vildagliptin","str_composition":"Vildagliptin 50.0000 Milligram (Mg)","str_indication":"Fixed Dose Combination Of Remogliflozin Etabonate & Vildagliptin Is Indicated In Adults Aged 18 Years And Older With Type 2 Diabetes Mellitus: ? To Improve Glycaemic Control When Metformin And One Of The Mono-Components Of Fixed Dose Combination Of Remogliflozin Etabonate & Vildagliptin Do Not Provide Adequate Glycaemic Control,  ? When Already Being Treated With The Free Combination Of Remogliflozin & Vildagliptin.","dt_closure_dt":"01-DEC-2020","str_man_unit_name":"Glenmark Pharmaceuticals Ltd."},{"str_drug_name":"Remogliflozin Etabonate+Vildagliptin","str_composition":"Remogliflozin Etabonate 100.0000 Milligram (Mg)","str_indication":"Fixed Dose Combination Of Remogliflozin Etabonate & Vildagliptin Is Indicated In Adults Aged 18 Years And Older With Type 2 Diabetes Mellitus: ? To Improve Glycaemic Control When Metformin And One Of The Mono-Components Of Fixed Dose Combination Of Remogliflozin Etabonate & Vildagliptin Do Not Provide Adequate Glycaemic Control,  ? When Already Being Treated With The Free Combination Of Remogliflozin & Vildagliptin.","dt_closure_dt":"01-DEC-2020","str_man_unit_name":"Glenmark Pharmaceuticals Ltd."},{"str_drug_name":"Renolazine Extend Release tablet (500mg)","str_composition":"","str_indication":"For Chronic Angina.","dt_closure_dt":"14.06.07","str_man_unit_name":""},{"str_drug_name":"Repaglinide 0.5/1.0mg+Voglibose 0.3/0.3mg Tablets","str_composition":"Repaglinide 100.0000 %,Voglibose 100.0000 %","str_indication":"It Used For Antidiabetic. 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Post Prandial Hyperglycemia) In Adults With Type 2 Diabetes Mellitus.","dt_closure_dt":"23-MAR-2020","str_man_unit_name":"Ajanta Pharma Limited"},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Repaglinide.... 1.0000 Milligram (Mg),Voglibose 0.3000 Milligram (Mg)","str_indication":"Indicated In Adults For The Treatment Of Type Ii Diabetes Mellitus, Who Have Inadequte Glycemic Control On Treatment With Repaglinide Alone Or Voglibose","dt_closure_dt":"10-SEP-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Repaglinide. 0.5000 Milligram (Mg),Voglibose 0.3000 Milligram (Mg)","str_indication":"Indicated In Adults For The Treatment Of Type Ii Diabetes Mellitus, Who Have Inadequte Glycemic Control On Treatment With Repaglinide Alone Or Voglibose","dt_closure_dt":"10-SEP-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Repaglinide.. 0.5000 Milligram (Mg),Voglibose 0.2000 Milligram (Mg)","str_indication":"Indicated In Adults For The Treatment Of Type Ii Diabetes Mellitus, Who Have Inadequte Glycemic Control On Treatment With Repaglinide Alone Or Voglibose","dt_closure_dt":"10-SEP-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Voglibose 0.2000 Milligram (Mg),Repaglinide 0.5000 Milligram (Mg)","str_indication":"Type 2 Diabetes Mellitus","dt_closure_dt":"17-DEC-2019","str_man_unit_name":"Torrent Pharmaceuticals Ltd."},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Repaglinide 1.0000 Milligram (Mg),Voglibose 0.2000 Milligram (Mg)","str_indication":"Type 2 Diabetes Mellitus","dt_closure_dt":"17-DEC-2019","str_man_unit_name":"Torrent Pharmaceuticals Ltd."},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Dichloromethane (Methylene Chloride) 0.0000 Q.S.,Voglibose 0.3000 Milligram (Mg),Repaglinide 0.5000 Milligram (Mg),Dibasic Calcium Phosphate (Anhydrous) 56.0000 Milligram (Mg),Poloxamer 188 (Kolliphor P 188) 6.0000 Milligram (Mg),Microcrystalline Cellulose 61.2000 Milligram (Mg),Povidone (P.V.P.K 30) 6.0000 Milligram (Mg),Starch (Maize Starch) 10.0000 Milligram (Mg),Colour Brilliant Blue Fcf Lake 0.5000 Milligram (Mg),Croscarmellose Sodium (Ac-Di- Sol) 4.0000 Milligram (Mg),Isopropyl Alchohol 0.0000 Q.S.,Colloidal Anhydrous Silica (Aerosil 200 / Cabosil M-5p) 0.5000 Milligram (Mg),Croscarmellose Sodium (Ac-Di- Sol) 4.0000 Milligram (Mg),Magnesium Stearate 1.0000 Milligram (Mg),Instacoat Universal A05d02184 Blue 5.0000 Milligram (Mg),Isopropyl Alcohol 0.0000 Q.S.,Dichloromethane (Methylene Chloride) 0.0000 Q.S.","str_indication":"Repaglinide And Voglibose Combination Tablet Is Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control (Esp. Post Prandial Hyperglycemia) In Adults With Type 2 Diabetes Mellitus.","dt_closure_dt":"23-MAR-2020","str_man_unit_name":"Ajanta Pharma Limited"},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Voglibose 0.2000 Milligram (Mg),Repaglinide 0.5000 Milligram (Mg),Dibasic Calcium Phosphate (Anhydrous) 56.0000 Milligram (Mg),Poloxamer 188 (Kolliphor P 188) 6.0000 Milligram (Mg),Microcrystalline Cellulose 61.3000 Milligram (Mg),Povidone (P.V.P.K 30) 6.0000 Milligram (Mg),Starch (Maize Starch) 10.0000 Milligram (Mg),Colour Sunset Yellow Lake 0.5000 Milligram (Mg),Croscarmellose Sodium (Ac-Di- Sol) 4.0000 Milligram (Mg),Isopropyl Alchohol 0.0000 Q.S.,Dichloromethane (Methylene Chloride) 0.0000 Q.S.,Colloidal Anhydrous Silica (Aerosil 200 / Cabosil M-5p) 0.5000 Milligram (Mg),Croscarmellose Sodium (Ac-Di- Sol) 4.0000 Milligram (Mg),Magnesium Stearate 1.0000 Milligram (Mg),Wincoat Wt-1079 Orange 5.0000 Milligram (Mg),Isopropyl Alcohol 0.0000 Q.S.,Dichloromethane (Methylene Chloride) 0.0000 Q.S.","str_indication":"Repaglinide And Voglibose Combination Tablet Is Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control (Esp. Post Prandial Hyperglycemia) In Adults With Type 2 Diabetes Mellitus.","dt_closure_dt":"23-MAR-2020","str_man_unit_name":"Ajanta Pharma Limited"},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Repaglinide 1.0000 Milligram (Mg),Voglibose 0.3000 Milligram (Mg)","str_indication":"Type 2 Diabetes Mellitus","dt_closure_dt":"17-DEC-2019","str_man_unit_name":"Torrent Pharmaceuticals Ltd."},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Repaglinide 0.5000 Milligram (Mg),Voglibose 0.3000 Milligram (Mg)","str_indication":"Type 2 Diabetes Mellitus","dt_closure_dt":"17-DEC-2019","str_man_unit_name":"Torrent Pharmaceuticals Ltd."},{"str_drug_name":"Repaglinide+Voglibose","str_composition":"Repaglinide... 1.0000 Milligram (Mg),Voglibose 0.2000 Milligram (Mg)","str_indication":"Indicated In Adults For The Treatment Of Type Ii Diabetes Mellitus, Who Have Inadequte Glycemic Control On Treatment With Repaglinide Alone Or Voglibose","dt_closure_dt":"10-SEP-2021","str_man_unit_name":"AKUMS DRUGS & PHARMACEUTICALS LIMITED"},{"str_drug_name":"Repreterol tablets/syrups","str_composition":"Each tablet contains; repreterol-20mg, Each 5ml contains; repreterol-10mg.","str_indication":"","dt_closure_dt":"1987-January","str_man_unit_name":"German remedies"},{"str_drug_name":"Reproterol hydrochloride","str_composition":"","str_indication":"Bronchodilator- Indicated in the treatment of conditions involving reversible airways obstruction viz bronchial asthma, bronchitis etc.","dt_closure_dt":"1986-September","str_man_unit_name":"German remedies"},{"str_drug_name":"Reproterol respirator solution/aerosol/injection","str_composition":"Respirator solution-10mg/ml, Aerosol-each metered dose-0.50mg, Injection-0.09mg/ml (Reproterol hcl)","str_indication":"","dt_closure_dt":"1987-October","str_man_unit_name":"German remedies"},{"str_drug_name":"Reproterol tablet/elixir","str_composition":"Tablet-reproterol hcl-20mg, Elixir-reproterol hcl-10mg/5ml","str_indication":"","dt_closure_dt":"1987-October","str_man_unit_name":"German remedies"},{"str_drug_name":"Reserpine + clopamide + dihydroergocristine","str_composition":"","str_indication":"Diuretic","dt_closure_dt":"1971- October","str_man_unit_name":"Sandoz, Bombay"},{"str_drug_name":"Reserpine + clopamide + dihydroergocristine","str_composition":"Each tablet contains; Reserpine-0.1mg, clopamide-5mg, dihydroergocristine-0.5mg","str_indication":"","dt_closure_dt":"1972- January","str_man_unit_name":"Sandoz, Bombay"},{"str_drug_name":"Residronate sodium (35mg) once weekly","str_composition":"35mg","str_indication":"","dt_closure_dt":"19/03/2004","str_man_unit_name":"Cipla ltd."},{"str_drug_name":"Resperidone E.R. 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In Pre- Or Perimenopausal Women, Or In Men, The Aromatase Inhibitor Should Be Combined With A Luteinising Hormone-Releasing Hormone (Lhrh) Agonist.","dt_closure_dt":"02-JAN-2026","str_man_unit_name":"Sandoz Private Limited"},{"str_drug_name":"Ribociclib Film-Coated Tablets 200 Mg","str_composition":"Ribociclib Succinate 254.40 Mg Equivalent To Ribociclib 200.0000 Milligram (Mg)","str_indication":"Ribociclib Is (A Cyclin-Dependent Kinase Inhibitor, Cdki) Indicated For The Treatment Of Patients With Hormone Receptor (Hr)-Positive, Human Epidermal Growth Factor Receptor 2 (Her2) Negative (Locally) Advanced Or Metastatic Breast Cancer In Combination With An Aromatase Inhibitor Or Fulvestrant. 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rofecoxib-12.5mg,25mg.","str_indication":"Not to be used in children","dt_closure_dt":"25-09-2000","str_man_unit_name":"TPL, Ranbaxy, Unichem, Sun, Cadila, Kopran, Mepro, Cipla"},{"str_drug_name":"Roflumilast Tab 500 mcg","str_composition":"Each film coated tablet contains; roflumilast-500mcg","str_indication":"For the \"maintenance treatment of severe chronic obstructive pulmonary disease (COPD) (FEV1 post-bronchodilator less than 50% predicted) associated with chronic bronchitis in adult patients  with a history of frequent exacerbations as add on to bronchodilޡ\u0005","dt_closure_dt":"17.07.14","str_man_unit_name":"Takeda pharma, Hetero(24.6.15)"},{"str_drug_name":"Roflumilast Tablets 250 Mcg","str_composition":"Roflumilast 250.0000 Mcg","str_indication":"Indicated For The Treatment Of Severe Chronic Obstructive Pulmonary Disease (Copd) (Fev1 Post Bronchodilator Less Than 50% Predicted) Associated With Chronic Bronchitis In Adult Patients With A History Of Frequent Exacerbations As Add On To Bronchodilator Treatment.","dt_closure_dt":"10-MAR-2026","str_man_unit_name":"MSN Laboratories Private Limited"},{"str_drug_name":"Romiplostim","str_composition":"Romiplostim Drug Substance 0.3750 Milligram (Mg),Mannitol 30.0000 Milligram (Mg),Sucrose 15.0000 Milligram (Mg),L-Histidine 1.2000 Milligram (Mg),Polysorbate 20 0.0300 Milligram (Mg),Hydrochloric Acid 5.0000 Ph Adjustment","str_indication":"Idiopathic Thrombocytopanic Purpura","dt_closure_dt":"01-JUL-2021","str_man_unit_name":"Enzene Biosciences Ltd., Pune"},{"str_drug_name":"Romiplostim","str_composition":"Romiplostim Drug Substance 0.2300 Milligram (Mg),Mannitol 18.0000 Milligram (Mg),Sucrose 9.0000 Milligram (Mg),L-Histidine 0.7000 Milligram (Mg),Polysorbate 20 0.0200 Milligram (Mg),Hydrochloric Acid 5.0000 Ph Adjustment","str_indication":"Idiopathic Thrombocytopanic Purpura","dt_closure_dt":"01-JUL-2021","str_man_unit_name":"Enzene Biosciences Ltd., Pune"},{"str_drug_name":"Romiplostim","str_composition":"Mannitol 50.0000 Milligram (Mg),Romiplostim Drug Substance 0.6250 Milligram (Mg),Sucrose 25.0000 Milligram (Mg),L-Histidine 1.9000 Milligram (Mg),Polysorbate 20 0.0500 Milligram (Mg),Hydrochloric Acid 5.0000 Ph Adjustment","str_indication":"Idiopathic Thrombocytopanic Purpura","dt_closure_dt":"01-JUL-2021","str_man_unit_name":"Enzene Biosciences Ltd., Pune"},{"str_drug_name":"Romiplostim Drug Substance","str_composition":"NA","str_indication":"NA","dt_closure_dt":"01-JUL-2021","str_man_unit_name":"Enzene Biosciences Ltd., Pune"},{"str_drug_name":"Romiplostim, Romiplostim Drug Substance, Mannitol, Sucrose, L-Histidine, Polysorbate 20, Hydrochloric Acid, Romiplostim, , , , , , , Romiplostim, , , , , , ","str_composition":"NA","str_indication":"NA","dt_closure_dt":"01-JUL-2021","str_man_unit_name":"Enzene Biosciences Ltd., Pune"},{"str_drug_name":"Romosozumab Injection","str_composition":"Romosozumab 90.0000 Mg/Ml","str_indication":"Treatment Of Postmenopausal Women With Osteoporosis At High Risk For Fracture","dt_closure_dt":"06-MAY-2021","str_man_unit_name":"Amgen Technology Pvt. Ltd."},{"str_drug_name":"Romosozumab (R-Dna Origin) Injection 90 Mg/Ml","str_composition":"Polysorbate 80 0.0700 Milligram (Mg),Acetate 3.8000 Milligram (Mg),Sucrose 70.0000 Milligram (Mg),Calcium 0.6100 Milligram (Mg),Romosozumab 105.0000 Milligram (Mg)","str_indication":"Treatment Of Postmenopausal Women With Osteoporosis At High Risk For Fracture Romosozumab Is Indicated For The Treatment Of Osteoporosis In Postmenopausal Women At High Risk For Fracture, Defined As A History Of Osteoporotic Fracture, Or Multiple Risk Factors For Fracture; Or Patients Who Have Failed Or Are Intolerant To Other Available Osteoporosis Therapy. Limitations Of Use The Anabolic Effect Of Romosozumab Wanes After 12 Monthly Doses Of Therapy. Therefore, The Duration Of Romosozumab Use Should Be Limited To 12 Monthly Doses. If Osteoporosis Therapy Remains Warranted, Continued Therapy With An Anti-Resorptive Agent Should Be Considered. Two 105 Mg/1.17 Ml Single Use Prefilled Syringes Are Required To Administer The Recommended 210 Mg Dose Of Romosozumab","dt_closure_dt":"11-JAN-2022","str_man_unit_name":"Dr. Reddys Laboratories Limited  "},{"str_drug_name":"R(+) Ondansetron (2mg/4mg) tablet","str_composition":"Each tablet contains; R(+) ondansetron Hcl.2H2O eq.to R(+) ondansetron-2mg, 4mg","str_indication":"For the treatment of chemotherapy induced nausea and vomiting.","dt_closure_dt":"15/04/2005","str_man_unit_name":"Emcure pharma ltd."},{"str_drug_name":"R-Ondansetron (As Hcl. Dihydrate) (1mg/ml) injection","str_composition":"","str_indication":"Chemotherapy induced nausea & vomiting.","dt_closure_dt":"12.01.07","str_man_unit_name":""},{"str_drug_name":"R(-) Ondansetron oral Solution (1mg/5ml)","str_composition":"Each 5ml of oral solution contains; R(-) ondansetron Hcl eq.to R(-) ondansetron-1mg","str_indication":"For Chemotherapy induced nausea and vomiting.","dt_closure_dt":"27/05/2005","str_man_unit_name":"Emcure pharma ltd."},{"str_drug_name":"Ropinirole 6mg ER Tablets (Addl. Strength)","str_composition":"","str_indication":"Same as approved","dt_closure_dt":"06.02.10","str_man_unit_name":""},{"str_drug_name":"Ropinirole ER Tablet 1 mg. 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Major Nerve Block; Local Infiltration And Epidural Continuous Infusion Or Intermittent Bolus, E.G., Postoperative Or Labor; Local Infiltration.","dt_closure_dt":"01-OCT-2025","str_man_unit_name":"Amneal Pharmaceuticals Pvt.Ltd."},{"str_drug_name":"Ropivacaine Injection, Ip 2 Mg/Ml (200 Mg/100 Ml), 2 Mg/Ml (400 Mg/200 Ml) & 5 Mg/Ml (500 Mg/100 Ml)","str_composition":"Ropivacaine Hydrochloride Equivalent To Anhydrous Ropivacaine Hydrochloride 2.0000 Milligram (Mg)","str_indication":"Indicated For Production Of Local Or Regional Anesthesia For Surgery And For Acute Pain Management, Epidural Block For Surgery Including Caesarean Section; Major Nerve Block; Local Infiltration And Epidural Continuous Infusion Or Intermittent Bolus, E.G., Postoperative Or Labor; Local Infiltration.","dt_closure_dt":"01-OCT-2025","str_man_unit_name":"Amneal Pharmaceuticals Pvt.Ltd."},{"str_drug_name":"Rosaxacin","str_composition":"Each capsule contains; rosoxacin-150mg","str_indication":"Oral anti-gonococcal agent- Indicated in the treatment of gonorrheal urethritis","dt_closure_dt":"1982-July","str_man_unit_name":"Win-medicare"},{"str_drug_name":"Rosiglitazone 1mg + Metofmin Hcl 500mg tablet (additional strength)","str_composition":"","str_indication":"As approved","dt_closure_dt":"08.02.07","str_man_unit_name":""},{"str_drug_name":"Rosiglitazone (as maleate)2mg + Glibenclamide 5mg + MetFormin 500mg table","str_composition":"Each film coated tablet contains; glibenclamide IP-5mg, metformin Hcl IP-500mg, Rosiglitazone maleate eq.to rosiglitazone-2mg","str_indication":"As 3rd line treatment of type-II diabetes mellitus when diet, excercise and the single agents and the second line therapy with two drugs do not result in adequate glycemic control.","dt_closure_dt":"08/08/2006","str_man_unit_name":"Sun pharma"},{"str_drug_name":"Rosiglitazone + glimepiride tab","str_composition":"Each film coated tab contains rosiglitazone maleate eq.to rosiglitazone-2mg, glimepiride-1mg","str_indication":"Type-II diabetes mellitus where diet, exercise & single agent do not result in adequate glycemic control.","dt_closure_dt":"14-11-2002","str_man_unit_name":"Glenmark"},{"str_drug_name":"Rosiglitazone maleate tablets","str_composition":"Each film coated tablet contains; rosiglitazone maleate eq.to 1mg,2mg,4mg,8mg of rosiglitazone.","str_indication":"By RMP- for treatment of type-II diabetes mellitus as mono therapy & adjunct to diet.","dt_closure_dt":"28-06-2000","str_man_unit_name":"Smith kline beecham, torrent, Dr. reddy"},{"str_drug_name":"Rosiglitazone + metformin (SR) tab","str_composition":"Rosiglitazone-2mg,4mg, metformin Sr-1000mg","str_indication":"RMP- For the treatment of patients with type-2 diabetes mellitus when diet exercise and the single agent do not result in adequate glycemic control.","dt_closure_dt":"20-05-2003","str_man_unit_name":"TPL"},{"str_drug_name":"Rosiglitazone + metformin (SR) tab","str_composition":"Each uncoated tab contains; 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(Additional Strength)","str_composition":"","str_indication":"For the treatment of patients with primary hypercholesterolemia.","dt_closure_dt":"05.12.11","str_man_unit_name":""},{"str_drug_name":"Rosuvastatin Calcium Tablet (Additional Indication)","str_composition":"","str_indication":"Risk reduction of MI stroke and arterial evascularisation procedure in patients without clinically evident CHD but with multiple risk factor.","dt_closure_dt":"24.05.10","str_man_unit_name":""},{"str_drug_name":"Rosuvastatin Calcium tablets 5/10/20/40mg (Addl. 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As adjunct to diet to reduce Total-C, LDL-C, and ApoB levels in adolesent boys and girls, who are at least one year post-menarche, 10-17 years of age with heterozygous hypercholesterolemia if after an adequate trial of diet therapy the following findinޡ\u0005","dt_closure_dt":"05.04.11","str_man_unit_name":""},{"str_drug_name":"Rosuvastatin  Calcium+Teneligliptin","str_composition":"Rosuvastatin Calcium 10.0000 Milligram (Mg),Teneligliptin 20.0000 Milligram (Mg)","str_indication":"For The Treatment Of Dyslipidemia Associated With Type Ii Diabetes Mellitus","dt_closure_dt":"23-MAY-2022","str_man_unit_name":"Theon Pharmaceuticals Ltd"},{"str_drug_name":"Rosuvastatin  Calcium+Teneligliptin","str_composition":"Rosuvastatin  Calcium 5.0000 Milligram (Mg),Teneligliptin 20.0000 Milligram (Mg)","str_indication":"For The Treatment Of Dyslipidemia Associated With Type Ii Diabetes Mellitus","dt_closure_dt":"23-MAY-2022","str_man_unit_name":"Theon Pharmaceuticals Ltd"},{"str_drug_name":"Rosuvastatin  Calcium+Teneligliptin","str_composition":"Rosuvastatin Calcium 20.0000 Milligram (Mg),Teneligliptin 20.0000 Milligram (Mg)","str_indication":"For The Treatment Of Dyslipidemia Associated With Type Ii Diabetes Mellitus","dt_closure_dt":"23-MAY-2022","str_man_unit_name":"Theon Pharmaceuticals Ltd"},{"str_drug_name":"Rosuvastatin Sprinkle Capsules 10 Mg, 20 Mg And 40 Mg","str_composition":"Rosuvastatin Calcium 10.0000 Milligram (Mg)","str_indication":"Indicated As An Adjunctive Therapy To Diet For The Treatment Of Adult Patients With Hypertriglyceridemia. As An Adjunct To Diet For The Treatment Of Adult Patients With Primary Dysbetalipoproteinemia (Type Iii Hyperlipoproteinemia). As Adjunctive Therapy To Other Lipidlowering Treatments (E.G., Ldl Apheresis) Or Alone If Such Treatments Are Unavailable To Reduce Ldlc, Total-C, And Apob In Adult Patients With Homozygous Familial Hypercholesterolemia.","dt_closure_dt":"03-MAR-2022","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Rosuvastatin Sprinkle Capsules 10 Mg, 20 Mg And 40 Mg","str_composition":"Rosuvastatin Calcium 40.0000 Milligram (Mg)","str_indication":"Indicated As An Adjunctive Therapy To Diet For The Treatment Of Adult Patients With Hypertriglyceridemia. As An Adjunct To Diet For The Treatment Of Adult Patients With Primary Dysbetalipoproteinemia (Type Iii Hyperlipoproteinemia). As Adjunctive Therapy To Other Lipidlowering Treatments (E.G., Ldl Apheresis) Or Alone If Such Treatments Are Unavailable To Reduce Ldlc, Total-C, And Apob In Adult Patients With Homozygous Familial Hypercholesterolemia.","dt_closure_dt":"03-MAR-2022","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Rosuvastatin Sprinkle Capsules 10 Mg, 20 Mg And 40 Mg","str_composition":"Rosuvastatin Calcium 20.0000 Milligram (Mg)","str_indication":"Indicated As An Adjunctive Therapy To Diet For The Treatment Of Adult Patients With Hypertriglyceridemia. As An Adjunct To Diet For The Treatment Of Adult Patients With Primary Dysbetalipoproteinemia (Type Iii Hyperlipoproteinemia). As Adjunctive Therapy To Other Lipidlowering Treatments (E.G., Ldl Apheresis) Or Alone If Such Treatments Are Unavailable To Reduce Ldlc, Total-C, And Apob In Adult Patients With Homozygous Familial Hypercholesterolemia.","dt_closure_dt":"03-MAR-2022","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Rosuvastatin+Teneligliptin","str_composition":"Teneligliptin 20.0000 Milligram (Mg),Rosuvastatin 10.0000 Milligram (Mg)","str_indication":"Dyslipidemia Associated With Type Ii Diabetes Mellitus","dt_closure_dt":"08-MAR-2022","str_man_unit_name":"Synokem Pharmaceuticals Ltd"},{"str_drug_name":"Rotavirus Vaccine ( Live Attenuated, Oral)","str_composition":"Water For Injection 0.5000 Ml (Q.S),Human Albumin 0.3500 %,Trisodium Citrate Dihydrate 7.7500 Milligram (Mg),Trehalose 2.5000 Milligram (Mg),Vero Cell Derived Rotavirus 116e Bulk, Live Attenuated 10.0000 To The Power Of 5.0 Ffu,Dipotassium Hydrogen Orthophosphate 10.0000 Milligram (Mg),Potassium Dihydrogen Orthophosphate 1.6500 Milligram (Mg),Sucrose 250.0000 Milligram (Mg),Lactalbumin Hydrolysate (Lah) 2.5000 Milligram (Mg)","str_indication":"Active Immunization Of Infants From The Age Of 6-8 Weeks For Preventions Of Gastroenteritis Due To Rotavirus Infection.","dt_closure_dt":"08-MAR-2024","str_man_unit_name":"Bharat Biotech International Limited"},{"str_drug_name":"Rotavirus Vaccine (Live Attenuated, Oral)","str_composition":"Others 10.0000 Ffu,Neomycin Sulphate 15.0000 ?g/Ml,Kanamycin Acid Sulphate 15.0000 ?g/Ml,Surose 0.2500 Gram (G),Trehalose 2.5000 Milligram (Mg),Lactalbumin Hydrolysate 2.5000 Milligram (Mg),Human Albumin 0.3500 %,Di Potassium Hydrogen Orthophosphate/ Potassium Phosphate Dibasic 10.0000 Gram (G),Potassium  Di Hydrogen Orthophosphate/ Potassium Phosphate Monobasic 1.6500 Gram (G),Tri Sodium Citrate Dihydrate 7.7500 Milligram (Mg)","str_indication":"Prevention Of Rvge","dt_closure_dt":"04-SEP-2018","str_man_unit_name":"Bharat Biotech International Limited"},{"str_drug_name":"Rotavirus Vaccine (Live Attenuated, Oral)","str_composition":"Rotavirus 116e Bulk, Live 10.0000 To The Power Of 5.0 Ffu,Potassium Phosphate Monobasic 0.2580 Milligram (Mg),Potassium Phosphate Dibasic 0.6250 Milligram (Mg),Sucrose 39.0000 Milligram (Mg),Potassium L-Glutamate, Monohydrate 1.0000 Milligram (Mg),Neomycin Sulphate 15.0000 Micrograms (?g),Kanamycin Sulphate 15.0000 Micrograms (?g),Dulbecco?S Modified Eagle?S Medium (Dmem) 4.4000 Milligram (Mg),Water For Injection 0.5000 Ml To Q.S","str_indication":"Active Immunization Of Infants From The Age Of 6weeks For Prevention Of Gastroenteritis Due To Rotavirus Infection.","dt_closure_dt":"11-SEP-2024","str_man_unit_name":"Sapigen Biologix Private Limited"},{"str_drug_name":"Rotavirus Vaccine (Live Attenuated, Oral)","str_composition":"Rotavirus 116e Bulk, Live 10.0000 To The Power Of 5.0 Ffu,Potassium Phosphate Monobasic 0.2580 Milligram (Mg),Potassium Phosphate Dibasic 0.6250 Milligram (Mg),Sucrose 39.0000 Milligram (Mg),Potassium L-Glutamate, Monohydrate 1.0000 Milligram (Mg),Neomycin Sulphate 30.0000 Micrograms (?g),Kanamycin Sulphate 20.0000 Micrograms (?g),Dulbecco?S Modified Eagle?S Medium (Dmem) 4.4000 Milligram (Mg),Water For Injection 0.5000 Ml To Q.S","str_indication":"Active Immunization Of Infants From The Age Of 6 Weeks For The  Prevention Of Gastroenteritis Due To Rotavirus Infection.","dt_closure_dt":"01-AUG-2025","str_man_unit_name":"Bharat Biotech International Limited"},{"str_drug_name":"Rotavirus Vaccine ( Live Attenuated, Oral) Formulated Bulk","str_composition":"Vero Cell Derived Rotavirus 116e Bulk Live Attenuated 10.0000 To The Power Of 5.0 Ffu","str_indication":"NA","dt_closure_dt":"06-JUN-2024","str_man_unit_name":"Bharat Biotech International Limited"},{"str_drug_name":"Rotavirus Vaccine (Live Attenuated, Oral) Ip","str_composition":"Human Rotavirus, Live Attenuated, Rix4414 Strain 10.0000 Raise To 6 Ccid50,Sucrose 1.0730 Gram (G),Di-Sodium Adipate 132.7400 Milligram (Mg),Dmem- Dulbecco?S Modified Eagle Medium 2.2600 Milligram (Mg),Water For Injections Q.S. Ad 1.5000 Ml","str_indication":"Indicated For The Active Immunization Of Infants From The Age Of 6 Weeks For Prevention Of Gastro-Enteritis Due To Rotavirus Infection","dt_closure_dt":"09-DEC-2021","str_man_unit_name":"GLAXOSMITHKLINE PHARMACEUTICALS LIMITED"},{"str_drug_name":"Rotavirus Vaccine (Live Attenuated, Oral) Ip","str_composition":"Human Rotavirus, Live Attenuated, Rix4414 Strain 10.0000 Raise To 6.0 Ccid50,Sucrose 9.0000 Milligram (Mg),Dextran 18.0000 Milligram (Mg),Sorbitol 13.5000 Milligram (Mg),Amino Acids 9.0000 Milligram (Mg),Dmem- Dulbecco?S Modified Eagle Medium 2.2500 Milligram (Mg),Calcium Carbonate (Diluent) 60.0000 Milligram (Mg),Xanthan (Diluent) 2.5000 Milligram (Mg),Water For Injections Q.S. 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"},{"str_drug_name":"Semaglutide Injection","str_composition":"Semaglutide 1.3400 Mg/Ml,Disodium Phosphate, Dihydrate 1.4200 Mg/Ml,Propylene Glycol 14.0000 Mg/Ml,Phenol 5.5000 Mg/Ml,Hydrochloric Acid 1.0000 Q.S.,Sodium Hydroxide 1.0000 Q.S.,Water For Injections 1.0000 Q.S.","str_indication":"Semaglutide Injection (Ozempic�)  Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise ?\tAs Monotherapy When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications. ?\tIn Addition To Other Medicinal Products For The Treatment Of Diabetes.  For Trial Results With Respect To Combinations, Effects On Glycaemic Control, Cardiovascular Events And Kidney Events And The Populations Studied, See Sections 4.4 (Special Warnings And Precautions For Use), 4.5 (Drugs Interactions) And 5.1. (Mechanism Of Action)","dt_closure_dt":"26-SEP-2025","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Injection","str_composition":"Semaglutide 1.3400 Mg/Ml (4mg/3ml)","str_indication":"Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise ? As Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications. ? In Addition To Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"26-MAY-2026","str_man_unit_name":"Dr. Reddys Laboratories Limited"},{"str_drug_name":"Semaglutide Injection","str_composition":"Disodium Phosphate Dihydrate 1.4200 Mg/Ml,Propylene Glycol 14.0000 Mg/Ml,Phenol 5.5000 Mg/Ml,Sodium Hydroxide 1.0000 Q.S.,Water For Injections 1.0000 To Make 1.00 Ml,Semaglutide 1.3400 Mg/Ml,Hydrochloric Acid 1.0000 Q.S.","str_indication":"Wegovy Is Indicated As An Adjunct To A Reduced-Calorie Diet And Increased Physical Activity For Weight Management In Adolescents Ages 12 Years And Above With ? Obesity* And ? Body Weight Above 60 Kg. Treatment With Wegovy Should Be Discontinued And Re-Evaluated If Adolescent Patients Have Not Reduced Their Bmi By At Least 5% After 12 Weeks On The 2.4 Mg Or Maximum Tolerated Dose. *Obesity (Bmi ?95th Percentile) As Defined On Sex- And Age-Specific Bmi Growth Charts (Cdc.Gov) (See Table 1).","dt_closure_dt":"05-MAY-2026","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Injection [0.25mg {(1mg /1.5ml) (0.68 Mg/Ml)}, 0.5mg {(2mg/1.5ml) (1.34 Mg/Ml)}, 1mg {(4mg/3ml) (1.34 Mg/Ml)}, 1.7mg {(6.8mg/3ml) (2.27 Mg/Ml)} & 2.4mg {(9.6mg/3ml) (3.2 Mg/Ml)}]","str_composition":"Semaglutide 1.7000 Milligram (Mg)","str_indication":"It Is Indicated As An Adjunct To A Reduced Calorie Diet And Increased Physical Activity For Chronic Weight Management In Adults With An Initial Body Mass Index (Bmi) Of ? 30 Kg/M2 Or Greater (Obesity) Or ? 27 Kg/M2 Or Greater (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Type 2 Diabetes Mellitus, Or Dyslipidemia)","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Alkem Laboratories Ltd. "},{"str_drug_name":"Semaglutide Injection [0.25mg {(1mg /1.5ml) (0.68 Mg/Ml)}, 0.5mg {(2mg/1.5ml) (1.34 Mg/Ml)}, 1mg {(4mg/3ml) (1.34 Mg/Ml)}, 1.7mg {(6.8mg/3ml) (2.27 Mg/Ml)} & 2.4mg {(9.6mg/3ml) (3.2 Mg/Ml)}]","str_composition":"Semaglutide 0.5000 Milligram (Mg)","str_indication":"It Is Indicated As An Adjunct To A Reduced Calorie Diet And Increased Physical Activity For Chronic Weight Management In Adults With An Initial Body Mass Index (Bmi) Of ? 30 Kg/M2 Or Greater (Obesity) Or ? 27 Kg/M2 Or Greater (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Type 2 Diabetes Mellitus, Or Dyslipidemia)","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Alkem Laboratories Ltd. "},{"str_drug_name":"Semaglutide Injection [0.25mg {(1mg /1.5ml) (0.68 Mg/Ml)}, 0.5mg {(2mg/1.5ml) (1.34 Mg/Ml)}, 1mg {(4mg/3ml) (1.34 Mg/Ml)}, 1.7mg {(6.8mg/3ml) (2.27 Mg/Ml)} & 2.4mg {(9.6mg/3ml) (3.2 Mg/Ml)}]","str_composition":"Semaglutide 1.0000 Milligram (Mg)","str_indication":"It Is Indicated As An Adjunct To A Reduced Calorie Diet And Increased Physical Activity For Chronic Weight Management In Adults With An Initial Body Mass Index (Bmi) Of ? 30 Kg/M2 Or Greater (Obesity) Or ? 27 Kg/M2 Or Greater (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Type 2 Diabetes Mellitus, Or Dyslipidemia)","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Alkem Laboratories Ltd. "},{"str_drug_name":"Semaglutide Injection [0.25mg {(1mg /1.5ml) (0.68 Mg/Ml)}, 0.5mg {(2mg/1.5ml) (1.34 Mg/Ml)}, 1mg {(4mg/3ml) (1.34 Mg/Ml)}, 1.7mg {(6.8mg/3ml) (2.27 Mg/Ml)} & 2.4mg {(9.6mg/3ml) (3.2 Mg/Ml)}]","str_composition":"Semaglutide 0.2500 Milligram (Mg)","str_indication":"It Is Indicated As An Adjunct To A Reduced Calorie Diet And Increased Physical Activity For Chronic Weight Management In Adults With An Initial Body Mass Index (Bmi) Of ? 30 Kg/M2 Or Greater (Obesity) Or ? 27 Kg/M2 Or Greater (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Type 2 Diabetes Mellitus, Or Dyslipidemia)","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Alkem Laboratories Ltd. "},{"str_drug_name":"Semaglutide Injection [0.25mg {(1mg /1.5ml) (0.68 Mg/Ml)}, 0.5mg {(2mg/1.5ml) (1.34 Mg/Ml)}, 1mg {(4mg/3ml) (1.34 Mg/Ml)}, 1.7mg {(6.8mg/3ml) (2.27 Mg/Ml)} & 2.4mg {(9.6mg/3ml) (3.2 Mg/Ml)}]","str_composition":"Semaglutide 2.4000 Milligram (Mg)","str_indication":"It Is Indicated As An Adjunct To A Reduced Calorie Diet And Increased Physical Activity For Chronic Weight Management In Adults With An Initial Body Mass Index (Bmi) Of ? 30 Kg/M2 Or Greater (Obesity) Or ? 27 Kg/M2 Or Greater (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Type 2 Diabetes Mellitus, Or Dyslipidemia)","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Alkem Laboratories Ltd. "},{"str_drug_name":"Semaglutide Injection 0.68 Mg/Ml (1 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (2 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (4 Mg/3 Ml Prefilled Pen), 2.27 Mg/Ml (6.8 Mg/3 Ml Prefilled Pen) & 3.2 Mg/Ml (9.6 Mg/3 Ml Prefilled Pen)","str_composition":"Semaglutide 0.6800 Mg/Ml","str_indication":"It Is Indicated As An Adjunct To A Reduced Calorie Diet And Increased Physical Activity For Chronic Weight Management In Adults With An Initial Body Mass Index (Bmi) Of  ? 30 Kg/M2 Or Greater (Obesity) Or ? 27 Kg/M2 Or Greater (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Type 2 Diabetes Mellitus, Or Dyslipidemia).","dt_closure_dt":"20-APR-2026","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Semaglutide Injection 0.68 Mg/Ml (1 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (2 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (4 Mg/3 Ml Prefilled Pen), 2.27 Mg/Ml (6.8 Mg/3 Ml Prefilled Pen) & 3.2 Mg/Ml (9.6 Mg/3 Ml Prefilled Pen)","str_composition":"Semaglutide 2.2700 Mg/Ml","str_indication":"It Is Indicated As An Adjunct To A Reduced Calorie Diet And Increased Physical Activity For Chronic Weight Management In Adults With An Initial Body Mass Index (Bmi) Of  ? 30 Kg/M2 Or Greater (Obesity) Or ? 27 Kg/M2 Or Greater (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Type 2 Diabetes Mellitus, Or Dyslipidemia).","dt_closure_dt":"20-APR-2026","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Semaglutide Injection 0.68 Mg/Ml (1 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (2 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (4 Mg/3 Ml Prefilled Pen), 2.27 Mg/Ml (6.8 Mg/3 Ml Prefilled Pen) & 3.2 Mg/Ml (9.6 Mg/3 Ml Prefilled Pen)","str_composition":"Semaglutide 3.2000 Mg/Ml","str_indication":"It Is Indicated As An Adjunct To A Reduced Calorie Diet And Increased Physical Activity For Chronic Weight Management In Adults With An Initial Body Mass Index (Bmi) Of  ? 30 Kg/M2 Or Greater (Obesity) Or ? 27 Kg/M2 Or Greater (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Type 2 Diabetes Mellitus, Or Dyslipidemia).","dt_closure_dt":"20-APR-2026","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Semaglutide Injection 0.68 Mg/Ml (1 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (2 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (4 Mg/3 Ml Prefilled Pen), 2.27 Mg/Ml (6.8 Mg/3 Ml Prefilled Pen) & 3.2 Mg/Ml (9.6 Mg/3 Ml Prefilled Pen)","str_composition":"Semaglutide 1.3400 Mg/Ml","str_indication":"It Is Indicated As An Adjunct To A Reduced Calorie Diet And Increased Physical Activity For Chronic Weight Management In Adults With An Initial Body Mass Index (Bmi) Of  ? 30 Kg/M2 Or Greater (Obesity) Or ? 27 Kg/M2 Or Greater (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Type 2 Diabetes Mellitus, Or Dyslipidemia).","dt_closure_dt":"20-APR-2026","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Semaglutide Injection 0.68 Mg/Ml (1 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (2 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (4 Mg/3 Ml Prefilled Pen) & 2.68 Mg/Ml (8 Mg/3 Ml Prefilled Pen)","str_composition":"Semaglutide 0.6800 Mg/Ml","str_indication":"Semaglutide Is A Glucagon-Like Peptide 1 (Glp-1) Receptor Agonist Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise ?\tAs Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications ?\tIn Addition To Other Medicinal Products For The Treatment Of Diabetes","dt_closure_dt":"20-APR-2026","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Semaglutide Injection 0.68 Mg/Ml (1 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (2 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (4 Mg/3 Ml Prefilled Pen) & 2.68 Mg/Ml (8 Mg/3 Ml Prefilled Pen)","str_composition":"Semaglutide 2.6800 Mg/Ml","str_indication":"Semaglutide Is A Glucagon-Like Peptide 1 (Glp-1) Receptor Agonist Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise ?\tAs Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications ?\tIn Addition To Other Medicinal Products For The Treatment Of Diabetes","dt_closure_dt":"20-APR-2026","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Semaglutide Injection 0.68 Mg/Ml (1 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (2 Mg/1.5 Ml Prefilled Pen), 1.34 Mg/Ml (4 Mg/3 Ml Prefilled Pen) & 2.68 Mg/Ml (8 Mg/3 Ml Prefilled Pen)","str_composition":"Semaglutide 1.3400 Mg/Ml","str_indication":"Semaglutide Is A Glucagon-Like Peptide 1 (Glp-1) Receptor Agonist Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise ?\tAs Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications ?\tIn Addition To Other Medicinal Products For The Treatment Of Diabetes","dt_closure_dt":"20-APR-2026","str_man_unit_name":"INTAS PHARMACEUTICALS LTD"},{"str_drug_name":"Semaglutide Injection 2mg/1.5ml (1.34mg/Ml) & 4mg/3ml (1.34mg/Ml)","str_composition":"Semaglutide 4.0000 Milligram (Mg)","str_indication":"Semaglutide is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet andexercise as monotherapy, when metformin is considered inappropriate due to intolerance or contraindications. In addition to other medicinal products for the treatment of diabetes.","dt_closure_dt":"10-DEC-2025","str_man_unit_name":"Alkem Laboratories Ltd. "},{"str_drug_name":"Semaglutide Injection 2mg/1.5ml (1.34mg/Ml) & 4mg/3ml (1.34mg/Ml)","str_composition":"Semaglutide 2.0000 Milligram (Mg)","str_indication":"Semaglutide is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet andexercise as monotherapy, when metformin is considered inappropriate due to intolerance or contraindications. In addition to other medicinal products for the treatment of diabetes.","dt_closure_dt":"10-DEC-2025","str_man_unit_name":"Alkem Laboratories Ltd. "},{"str_drug_name":"Semaglutide Injection 2mg/1.5ml (1.34mg/Ml) ,4mg/3ml (1.34mg/Ml)  And 8mg/3ml (2.68mg/Ml)","str_composition":"Semaglutide 4.0000 Mg/3ml","str_indication":"Semaglutide Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise ?\tAs Monotherapy When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications ?\tIn Addition To Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"20-APR-2026","str_man_unit_name":"Hetero Labs Limited"},{"str_drug_name":"Semaglutide Injection 2mg/1.5ml (1.34mg/Ml) ,4mg/3ml (1.34mg/Ml)  And 8mg/3ml (2.68mg/Ml)","str_composition":"Semaglutide 2.0000 Mg /1.5ml","str_indication":"Semaglutide Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise ?\tAs Monotherapy When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications ?\tIn Addition To Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"20-APR-2026","str_man_unit_name":"Hetero Labs Limited"},{"str_drug_name":"Semaglutide Injection 2mg/1.5ml (1.34mg/Ml) ,4mg/3ml (1.34mg/Ml)  And 8mg/3ml (2.68mg/Ml)","str_composition":"Semaglutide 8.0000 Mg/3ml","str_indication":"Semaglutide Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise ?\tAs Monotherapy When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications ?\tIn Addition To Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"20-APR-2026","str_man_unit_name":"Hetero Labs Limited"},{"str_drug_name":"Semaglutide Injection 2mg/3ml (0.68mg/Ml), 4mg/3ml (1.34mg/Ml) & 8mg/3ml (2.68mg/Ml)","str_composition":"Semaglutide 1.3400 Mg/Ml","str_indication":"It Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes As An Adjunct To Diet And Exercise. 1. As Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications. 2. In Addition To The Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"23-FEB-2026","str_man_unit_name":"MSN Laboratories Private Limited"},{"str_drug_name":"Semaglutide Injection 2mg/3ml (0.68mg/Ml), 4mg/3ml (1.34mg/Ml) & 8mg/3ml (2.68mg/Ml)","str_composition":"Semaglutide 0.6800 Mg/Ml","str_indication":"It Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes As An Adjunct To Diet And Exercise. 1. As Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications. 2. In Addition To The Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"23-FEB-2026","str_man_unit_name":"MSN Laboratories Private Limited"},{"str_drug_name":"Semaglutide Injection 2mg/3ml (0.68mg/Ml), 4mg/3ml (1.34mg/Ml) & 8mg/3ml (2.68mg/Ml)","str_composition":"Semaglutide 2.6800 Mg/Ml","str_indication":"It Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes As An Adjunct To Diet And Exercise. 1. As Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications. 2. In Addition To The Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"23-FEB-2026","str_man_unit_name":"MSN Laboratories Private Limited"},{"str_drug_name":"Semaglutide Injection 2 Mg {(8mg/3ml) (2.68mg/Ml)}","str_composition":"Semaglutide 2.0000 Milligram (Mg)","str_indication":"Semaglutide is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet andexercise as monotherapy, when metformin is considered inappropriate due to intolerance or contraindications. In addition to other medicinal products for the treatment of diabetes.","dt_closure_dt":"10-DEC-2025","str_man_unit_name":"Alkem Laboratories Ltd. "},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Semaglutide 1.0000 Mg/Ml","str_indication":"Semaglutide  Solution  For  Injection  Is  Indicated  As  An  Adjunct  To  A  Reducedcalorie  Diet  And Increased Physical Activity For Chronic Weight Managementin Adults With An Initial Body Mass Index (Bmi) Of\r\n30 Kg/M2or Greater (Obesity) Or\r\n27 Kg/M2or Greater (Overweight) In The Presence Of At Least Oneweight-Related Comorbid Condition (E.G., Hypertension, Type 2diabetes Mellitus, Or Dyslipidemia)\r\nLimitation Of Use\r\nSemaglutide Solution For Injection Should Not Be Co-Administeredwith Other Semaglutide-Containing Products Or With Any Other Glp-1 Receptor Agonist.\r\nThe Safety And Effectiveness Of Semaglutide In Combination Withother Products Intended For   Weight   Loss,   Including   Prescriptiondrugs,   Over-The-Counter   Drugs,   And   Herbal Preparations, Have Notbeen Established.\r\nSemaglutide  Solution  For  Injection  Has  Not  Been  Studied  In  Patientswith  A  History  Of Pancreatitis.","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Semaglutide 2.0000 Mg/Ml","str_indication":"Semaglutide  Solution  For  Injection  Is  Indicated  As  An  Adjunct  To  A  Reducedcalorie  Diet  And Increased Physical Activity For Chronic Weight Managementin Adults With An Initial Body Mass Index (Bmi) Of\r\n30 Kg/M2or Greater (Obesity) Or\r\n27 Kg/M2or Greater (Overweight) In The Presence Of At Least Oneweight-Related Comorbid Condition (E.G., Hypertension, Type 2diabetes Mellitus, Or Dyslipidemia)\r\nLimitation Of Use\r\nSemaglutide Solution For Injection Should Not Be Co-Administeredwith Other Semaglutide-Containing Products Or With Any Other Glp-1 Receptor Agonist.\r\nThe Safety And Effectiveness Of Semaglutide In Combination Withother Products Intended For   Weight   Loss,   Including   Prescriptiondrugs,   Over-The-Counter   Drugs,   And   Herbal Preparations, Have Notbeen Established.\r\nSemaglutide  Solution  For  Injection  Has  Not  Been  Studied  In  Patientswith  A  History  Of Pancreatitis.","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Semaglutide 3.2000 Mg/Ml","str_indication":"Semaglutide  Solution  For  Injection  Is  Indicated  As  An  Adjunct  To  A  Reducedcalorie  Diet  And Increased Physical Activity For Chronic Weight Managementin Adults With An Initial Body Mass Index (Bmi) Of\r\n30 Kg/M2or Greater (Obesity) Or\r\n27 Kg/M2or Greater (Overweight) In The Presence Of At Least Oneweight-Related Comorbid Condition (E.G., Hypertension, Type 2diabetes Mellitus, Or Dyslipidemia)\r\nLimitation Of Use\r\nSemaglutide Solution For Injection Should Not Be Co-Administeredwith Other Semaglutide-Containing Products Or With Any Other Glp-1 Receptor Agonist.\r\nThe Safety And Effectiveness Of Semaglutide In Combination Withother Products Intended For   Weight   Loss,   Including   Prescriptiondrugs,   Over-The-Counter   Drugs,   And   Herbal Preparations, Have Notbeen Established.\r\nSemaglutide  Solution  For  Injection  Has  Not  Been  Studied  In  Patientswith  A  History  Of Pancreatitis.","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Semaglutide 0.6800 Mg/Ml,Disodium Phosphate, Dihydrate 1.4200 Mg/Ml,Propylene Glycol 14.0000 Mg/Ml,Phenol 5.5000 Mg/Ml,Hydrochloric Acid 1.0000 Q.S.,Sodium Hydroxide 1.0000 Q.S.,Water For Injections 1.0000 Ml","str_indication":"Wegovy Is Indicated As An Adjunct To A Reduced-Calorie Diet And Increased Physical Activity For Weight Management, Including Weight Loss And Weight Maintenance, In Adults With An Initial Body Mass Index (Bmi) Of ? ?30 Kg/M2, Or ? ?27 Kg/M2 To <30 Kg/M2 In The Presence Of At Least One Weight-Related Comorbidity E.G. Dysglycaemia (Prediabetes Or Type 2 Diabetes Mellitus), Hypertension, Dyslipidaemia, Obstructive Sleep Apnoea Or Cardiovascular Disease.","dt_closure_dt":"17-OCT-2022","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Disodium Phosphate, Dihydrate 1.4200 Mg/Ml,Propylene Glycol 14.0000 Mg/Ml,Phenol 5.5000 Mg/Ml,Hydrochloric Acid 1.0000 Q.S.,Sodium Hydroxide 1.0000 Q.S.,Water For Injections 1.0000 Ml,Semaglutide 1.3400 Mg/Ml","str_indication":"Wegovy Is Indicated As An Adjunct To A Reduced-Calorie Diet And Increased Physical Activity For Weight Management, Including Weight Loss And Weight Maintenance, In Adults With An Initial Body Mass Index (Bmi) Of ? ?30 Kg/M2, Or ? ?27 Kg/M2 To <30 Kg/M2 In The Presence Of At Least One Weight-Related Comorbidity E.G. Dysglycaemia (Prediabetes Or Type 2 Diabetes Mellitus), Hypertension, Dyslipidaemia, Obstructive Sleep Apnoea Or Cardiovascular Disease.","dt_closure_dt":"17-OCT-2022","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Semaglutide 1.3400 Mg/Ml,Disodium Phosphate, Dihydrate 1.4200 Mg/Ml,Propylene Glycol 14.0000 Mg/Ml,Phenol 5.5000 Mg/Ml,Hydrochloric Acid 1.0000 Q.S.,Sodium Hydroxide 1.0000 Q.S.,Water For Injections 1.0000 Ml","str_indication":"Wegovy Is Indicated As An Adjunct To A Reduced-Calorie Diet And Increased Physical Activity For Weight Management, Including Weight Loss And Weight Maintenance, In Adults With An Initial Body Mass Index (Bmi) Of ? ?30 Kg/M2, Or ? ?27 Kg/M2 To <30 Kg/M2 In The Presence Of At Least One Weight-Related Comorbidity E.G. Dysglycaemia (Prediabetes Or Type 2 Diabetes Mellitus), Hypertension, Dyslipidaemia, Obstructive Sleep Apnoea Or Cardiovascular Disease.","dt_closure_dt":"17-OCT-2022","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Semaglutide 2.2700 Mg/Ml,Disodium Phosphate, Dihydrate 1.4200 Mg/Ml,Propylene Glycol 14.0000 Mg/Ml,Phenol 5.5000 Mg/Ml,Hydrochloric Acid 1.0000 Q.S.,Sodium Hydroxide 1.0000 Q.S.,Water For Injections 1.0000 Ml","str_indication":"Wegovy Is Indicated As An Adjunct To A Reduced-Calorie Diet And Increased Physical Activity For Weight Management, Including Weight Loss And Weight Maintenance, In Adults With An Initial Body Mass Index (Bmi) Of ? ?30 Kg/M2, Or ? ?27 Kg/M2 To <30 Kg/M2 In The Presence Of At Least One Weight-Related Comorbidity E.G. Dysglycaemia (Prediabetes Or Type 2 Diabetes Mellitus), Hypertension, Dyslipidaemia, Obstructive Sleep Apnoea Or Cardiovascular Disease.","dt_closure_dt":"17-OCT-2022","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Semaglutide 3.2000 Mg/Ml,Disodium Phosphate, Dihydrate 1.4200 Mg/Ml,Propylene Glycol 14.0000 Mg/Ml,Phenol 5.5000 Mg/Ml,Hydrochloric Acid 1.0000 Q.S.,Sodium Hydroxide 1.0000 Q.S.,Water For Injections 1.0000 Ml","str_indication":"Wegovy Is Indicated As An Adjunct To A Reduced-Calorie Diet And Increased Physical Activity For Weight Management, Including Weight Loss And Weight Maintenance, In Adults With An Initial Body Mass Index (Bmi) Of ? ?30 Kg/M2, Or ? ?27 Kg/M2 To <30 Kg/M2 In The Presence Of At Least One Weight-Related Comorbidity E.G. Dysglycaemia (Prediabetes Or Type 2 Diabetes Mellitus), Hypertension, Dyslipidaemia, Obstructive Sleep Apnoea Or Cardiovascular Disease.","dt_closure_dt":"17-OCT-2022","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Semaglutide 0.5000 Mg/Ml","str_indication":"Semaglutide  Solution  For  Injection  Is  Indicated  As  An  Adjunct  To  A  Reducedcalorie  Diet  And Increased Physical Activity For Chronic Weight Managementin Adults With An Initial Body Mass Index (Bmi) Of\r\n30 Kg/M2or Greater (Obesity) Or\r\n27 Kg/M2or Greater (Overweight) In The Presence Of At Least Oneweight-Related Comorbid Condition (E.G., Hypertension, Type 2diabetes Mellitus, Or Dyslipidemia)\r\nLimitation Of Use\r\nSemaglutide Solution For Injection Should Not Be Co-Administeredwith Other Semaglutide-Containing Products Or With Any Other Glp-1 Receptor Agonist.\r\nThe Safety And Effectiveness Of Semaglutide In Combination Withother Products Intended For   Weight   Loss,   Including   Prescriptiondrugs,   Over-The-Counter   Drugs,   And   Herbal Preparations, Have Notbeen Established.\r\nSemaglutide  Solution  For  Injection  Has  Not  Been  Studied  In  Patientswith  A  History  Of Pancreatitis.","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Semaglutide Solution For Injection","str_composition":"Semaglutide 2.2700 Mg/Ml","str_indication":"Semaglutide  Solution  For  Injection  Is  Indicated  As  An  Adjunct  To  A  Reducedcalorie  Diet  And Increased Physical Activity For Chronic Weight Managementin Adults With An Initial Body Mass Index (Bmi) Of\r\n30 Kg/M2or Greater (Obesity) Or\r\n27 Kg/M2or Greater (Overweight) In The Presence Of At Least Oneweight-Related Comorbid Condition (E.G., Hypertension, Type 2diabetes Mellitus, Or Dyslipidemia)\r\nLimitation Of Use\r\nSemaglutide Solution For Injection Should Not Be Co-Administeredwith Other Semaglutide-Containing Products Or With Any Other Glp-1 Receptor Agonist.\r\nThe Safety And Effectiveness Of Semaglutide In Combination Withother Products Intended For   Weight   Loss,   Including   Prescriptiondrugs,   Over-The-Counter   Drugs,   And   Herbal Preparations, Have Notbeen Established.\r\nSemaglutide  Solution  For  Injection  Has  Not  Been  Studied  In  Patientswith  A  History  Of Pancreatitis.","dt_closure_dt":"16-JAN-2026","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Semaglutide Solution For Injection 1.34 Mg/Ml (2 Mg/1.5 Ml)","str_composition":"Semaglutide 1.3400 Mg/Ml","str_indication":"Semaglutide Solution For Injection Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise\r\n As Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications.\r\n In Addition To Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"03-DEC-2025","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Semaglutide Solution For Injection 1.34 Mg/Ml (4 Mg/3 Ml)","str_composition":"Semaglutide 1.3400 Mg/Ml","str_indication":"Semaglutide Solution For Injection Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise\r\n As Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications.\r\n In Addition To Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"03-DEC-2025","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Semaglutide Solution For Injection 2.68 Mg/Ml (8 Mg/3 Ml)","str_composition":"Semaglutide 2.6800 Mg/Ml","str_indication":"Semaglutide Solution For Injection Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise\r\n As Monotherapy, When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications.\r\nIn Addition To Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"03-DEC-2025","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Semaglutide (Synthetic Origin)","str_composition":"Semaglutide 0.0000 Not Applicable (Na)","str_indication":"NA","dt_closure_dt":"03-DEC-2025","str_man_unit_name":"Sun Pharmaceutical Industries Limited"},{"str_drug_name":"Semaglutide Tablets","str_composition":"Semaglutide 3.0000 Milligram (Mg),Salcaprazate Sodium 300.0000 Milligram (Mg)","str_indication":"Rybelsus Is Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus","dt_closure_dt":"19-JAN-2024","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Tablets","str_composition":"Magnesium Stearate 9.7000 Milligram (Mg),Povidone K 90 8.0000 Milligram (Mg),Salcaprozate Sodium 300.0000 Milligram (Mg),Semaglutide 3.0000 Milligram (Mg),Cellulose, Microcrystalline 80.0000 Milligram (Mg)","str_indication":"Rybelsus� Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise. Rybelsus� Is Indicated To Reduce The Risk Of Major Adverse Cardiovascular Events (Cardiovascular Death, Non-Fatal Myocardial Infarction, Or Non-Fatal Stroke) In Adults With Type 2 Diabetes Mellitus And Established Cardiovascular Disease And/Or Chronic Kidney Disease.","dt_closure_dt":"29-JUL-2020","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Tablets","str_composition":"Semaglutide 3.0000 Milligram (Mg),Salcaprozate Sodium 300.0000 Milligram (Mg),Cellulose, Microcrystalline 80.0000 Milligram (Mg),Povidone K 90 8.0000 Milligram (Mg),Magnesium Stearate 9.7000 Milligram (Mg)","str_indication":"Rybelsus� Is Indicated For: ?\tAs An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus. ?\tTo Reduce The Risk Of Major Adverse Cardiovascular Events (Cardiovascular Death, Non-Fatal Myocardial Infarction Or Non-Fatal Stroke) In Adults With Type 2 Diabetes Mellitus And Established Cardiovascular Disease And/Or Chronic Kidney Disease.  Limitations Of Use ? Rybelsus� Has Not Been Studied In Patients With A History Of Pancreatitis. Consider Other Antidiabetic Therapies In Patients With A History Of Pancreatitis. [See Section 4.4 Special Warnings And Precautions] ? Rybelsus� Is Not Indicated For Use In Patients With Type 1 Diabetes Mellitus","dt_closure_dt":"09-FEB-2026","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Tablets","str_composition":"Povidone K 90 8.0000 Milligram (Mg),Salcaprozate Sodium 300.0000 Milligram (Mg),Semaglutide 14.0000 Milligram (Mg),Cellulose, Microcrystalline 80.0000 Milligram (Mg),Magnesium Stearate 9.7000 Milligram (Mg)","str_indication":"Rybelsus� Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise. Rybelsus� Is Indicated To Reduce The Risk Of Major Adverse Cardiovascular Events (Cardiovascular Death, Non-Fatal Myocardial Infarction, Or Non-Fatal Stroke) In Adults With Type 2 Diabetes Mellitus And Established Cardiovascular Disease And/Or Chronic Kidney Disease.","dt_closure_dt":"29-JUL-2020","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Tablets","str_composition":"Semaglutide 14.0000 Milligram (Mg),Salcaprazate Sodium 300.0000 Milligram (Mg)","str_indication":"Rybelsus Is Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus","dt_closure_dt":"19-JAN-2024","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Tablets","str_composition":"Semaglutide 14.0000 Milligram (Mg),Salcaprozate Sodium 300.0000 Milligram (Mg),Cellulose, Microcrystalline 80.0000 Milligram (Mg),Povidone K 90 8.0000 Milligram (Mg),Magnesium Stearate 9.7000 Milligram (Mg)","str_indication":"Rybelsus� Is Indicated For: ?\tAs An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus. ?\tTo Reduce The Risk Of Major Adverse Cardiovascular Events (Cardiovascular Death, Non-Fatal Myocardial Infarction Or Non-Fatal Stroke) In Adults With Type 2 Diabetes Mellitus And Established Cardiovascular Disease And/Or Chronic Kidney Disease.  Limitations Of Use ? Rybelsus� Has Not Been Studied In Patients With A History Of Pancreatitis. Consider Other Antidiabetic Therapies In Patients With A History Of Pancreatitis. [See Section 4.4 Special Warnings And Precautions] ? Rybelsus� Is Not Indicated For Use In Patients With Type 1 Diabetes Mellitus","dt_closure_dt":"09-FEB-2026","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Tablets","str_composition":"Semaglutide 7.0000 Milligram (Mg),Salcaprozate Sodium 300.0000 Milligram (Mg),Cellulose, Microcrystalline 80.0000 Milligram (Mg),Povidone K 90 8.0000 Milligram (Mg),Magnesium Stearate 9.7000 Milligram (Mg)","str_indication":"Rybelsus� Is Indicated For: ?\tAs An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus. ?\tTo Reduce The Risk Of Major Adverse Cardiovascular Events (Cardiovascular Death, Non-Fatal Myocardial Infarction Or Non-Fatal Stroke) In Adults With Type 2 Diabetes Mellitus And Established Cardiovascular Disease And/Or Chronic Kidney Disease.  Limitations Of Use ? Rybelsus� Has Not Been Studied In Patients With A History Of Pancreatitis. Consider Other Antidiabetic Therapies In Patients With A History Of Pancreatitis. [See Section 4.4 Special Warnings And Precautions] ? Rybelsus� Is Not Indicated For Use In Patients With Type 1 Diabetes Mellitus","dt_closure_dt":"09-FEB-2026","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Tablets","str_composition":"Salcaprozate Sodium 300.0000 Milligram (Mg),Semaglutide 7.0000 Milligram (Mg),Povidone K 90 8.0000 Milligram (Mg),Cellulose, Microcrystalline 80.0000 Milligram (Mg),Magnesium Stearate 9.7000 Milligram (Mg)","str_indication":"Rybelsus� Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise. Rybelsus� Is Indicated To Reduce The Risk Of Major Adverse Cardiovascular Events (Cardiovascular Death, Non-Fatal Myocardial Infarction, Or Non-Fatal Stroke) In Adults With Type 2 Diabetes Mellitus And Established Cardiovascular Disease And/Or Chronic Kidney Disease.","dt_closure_dt":"29-JUL-2020","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Tablets","str_composition":"Semaglutide 7.0000 Milligram (Mg),Salcaprazate Sodium 300.0000 Milligram (Mg)","str_indication":"Rybelsus Is Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus","dt_closure_dt":"19-JAN-2024","str_man_unit_name":"Novo Nordisk India Pvt Ltd"},{"str_drug_name":"Semaglutide Tablets 3 Mg, 7 Mg And 14 Mg","str_composition":"Semaglutide 3.0000 Milligram (Mg)","str_indication":"Semaglutide Is Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus As Monotherapy When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications; In Combination With Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"19-FEB-2026","str_man_unit_name":"Torrent Pharmaceuticals Ltd."},{"str_drug_name":"Semaglutide Tablets 3 Mg, 7 Mg And 14 Mg","str_composition":"Semaglutide 14.0000 Milligram (Mg)","str_indication":"Semaglutide Is Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus As Monotherapy When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications; In Combination With Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"19-FEB-2026","str_man_unit_name":"Torrent Pharmaceuticals Ltd."},{"str_drug_name":"Semaglutide Tablets 3 Mg, 7 Mg And 14 Mg","str_composition":"Semaglutide 7.0000 Milligram (Mg)","str_indication":"Semaglutide Is Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus As Monotherapy When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications; In Combination With Other Medicinal Products For The Treatment Of Diabetes.","dt_closure_dt":"19-FEB-2026","str_man_unit_name":"Torrent Pharmaceuticals Ltd."},{"str_drug_name":"Semaglutide Tablets 3 Mg, 7 Mg And 14 Mg","str_composition":"Semaglutide 7.0000 Milligram (Mg)","str_indication":"Oral Semaglutide Is A Glucagon Like Peptide 1 (Glp1) Receptor Agonist Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus. Also, In Combination With Other Medicinal Products For The Treatment Of Type 2 Diabetes. Limitations Of Use - Has Not Been Studied In Patients With A History Of Pancreatitis, Not Indicated For Use In Patients With Type 1 Diabetes Mellitus.","dt_closure_dt":"23-MAR-2026","str_man_unit_name":"Dr. Reddys Laboratories Limited  "},{"str_drug_name":"Semaglutide Tablets 3 Mg, 7 Mg And 14 Mg","str_composition":"Semaglutide 3.0000 Milligram (Mg)","str_indication":"Oral Semaglutide Is A Glucagon Like Peptide 1 (Glp1) Receptor Agonist Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus. Also, In Combination With Other Medicinal Products For The Treatment Of Type 2 Diabetes. Limitations Of Use - Has Not Been Studied In Patients With A History Of Pancreatitis, Not Indicated For Use In Patients With Type 1 Diabetes Mellitus.","dt_closure_dt":"23-MAR-2026","str_man_unit_name":"Dr. Reddys Laboratories Limited  "},{"str_drug_name":"Semaglutide Tablets 3 Mg, 7 Mg And 14 Mg","str_composition":"Semaglutide 14.0000 Milligram (Mg)","str_indication":"Oral Semaglutide Is A Glucagon Like Peptide 1 (Glp1) Receptor Agonist Indicated As An Adjunct To Diet And Exercise To Improve Glycemic Control In Adults With Type 2 Diabetes Mellitus. Also, In Combination With Other Medicinal Products For The Treatment Of Type 2 Diabetes. Limitations Of Use - Has Not Been Studied In Patients With A History Of Pancreatitis, Not Indicated For Use In Patients With Type 1 Diabetes Mellitus.","dt_closure_dt":"23-MAR-2026","str_man_unit_name":"Dr. Reddys Laboratories Limited  "},{"str_drug_name":"Semduramicin sodium 5% premix","str_composition":"Each kg of premix contains; semduramicin-50gm (eq.to semduramicin sod.)","str_indication":"","dt_closure_dt":"04/03/1998","str_man_unit_name":"Pfizer ltd."},{"str_drug_name":"Septopal beads and chains","str_composition":"","str_indication":"Indicated for the treatment of bone and soft tissue infections.","dt_closure_dt":"1985-January","str_man_unit_name":""},{"str_drug_name":"Seratrodast tablets 40mg/80mg","str_composition":"Each tablet contains; seratrodast-40mg, 80mg","str_indication":"As add-on therapy in bronchial asthma.","dt_closure_dt":"30.11.12","str_man_unit_name":"Zuventus healthcare ltd."},{"str_drug_name":"Serenoa repens caps.","str_composition":"Each soft gelatin cap contains; 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For Study Results With Respect To Combinations, Effects On Glycaemic Control And The Populations Studied, See Sections 4.4, 4.5 And 5.1. Weight Management Tirzepatide Is Indicated As An Adjunct To A Reduced-Calorie Diet And Increased Physical Activity For Weight Management, Including Weight Loss And Weight Maintenance, In Adults With An Initial Body Mass Index (Bmi) Of ? 30 Kg/M2 (Obesity) Or ? 27 Kg/M2 To < 30 Kg/M2 (Overweight) In The Presence Of At Least One Weight-Related Comorbid Condition (E.G., Hypertension, Dyslipidaemia, Obstructive Sleep Apnoea, Cardiovascular Disease, Prediabetes, Or Type 2 Diabetes Mellitus).","dt_closure_dt":"21-MAR-2025","str_man_unit_name":"Eli Lilly And Company"},{"str_drug_name":"Tirzepatide","str_composition":"Tirzepatide 5.0000 Milligram (Mg),Dibasic Sodium Phosphate Heptahydrate 0.8000 Milligram (Mg),Sodium Chloride 1.0500 Milligram (Mg),Glycerin 4.8000 Milligram (Mg),Benzyl Alcohol 5.4000 Milligram (Mg),Phenol 1.0800 Milligram (Mg),Hydrochloric Acid Solution 1.0000 Q.S.,Sodium Hydroxide Solution 1.0000 Q.S.,Water For Injection 1.0000 Q.S.","str_indication":"Type 2 Diabetes Mellitus Tirzepatide Is Indicated For The Treatment Of Adults With Insufficiently Controlled Type 2 Diabetes Mellitus As An Adjunct To Diet And Exercise, As Monotherapy When Metformin Is Considered Inappropriate Due To Intolerance Or Contraindications, In Addition To Other Medicinal Products For The Treatment Of Diabetes. For Study Results With Respect To Combinations, Effects On Glycaemic Control And The Populations Studied, See Sections 4.4, 4.5 And 5.1. 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For Study Results With Respect To Combinations, Effects On Glycaemic Control And The Populations Studied, See Sections 4.4, 4.5 And 5.1. 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Patients With Hormone Receptor Positive (Hr+) Breast Cancer Should Additionally Have Received Or Be Ineligible For Endocrine Therapy","dt_closure_dt":"26-MAR-2024","str_man_unit_name":"AstraZeneca Pharma India Limited"},{"str_drug_name":"Trastuzumab Deruxtecan Concentrate Solution For Infusion (Enhertu)","str_composition":"Trastuzumab Deruxtecan 107.0000 Milligram (Mg),Sucrose 482.0000 Milligram (Mg),L-Histidine 4.7600 Milligram (Mg),L-Histidine Hydrochloride Monohydrate 21.6000 Milligram (Mg),Polysorbate 80 1.6100 Milligram (Mg)","str_indication":"Enhertu Is Indicated For The Treatment Of Adult Patients With Locally Advanced Or Metastatic Her2-Positive Gastric Or Gastroesophageal Junction (Gej) Adenocarcinoma Who Have Received A Prior Anti-Her2-Based Regimen","dt_closure_dt":"26-MAR-2024","str_man_unit_name":"AstraZeneca Pharma India Limited"},{"str_drug_name":"Trastuzumab Deruxtecan Powder For Concentrate For Solution For Infusion","str_composition":"Trastuzumab Deruxtecan 100.0000 Mg/5ml,Sucrose 450.0000 Milligram (Mg),L-Histidine 4.4500 Milligram (Mg),L-Histidine Hydrochloride Monohydrate 20.2000 Milligram (Mg),Polysorbate 80 1.5000 Milligram (Mg)","str_indication":"Trastuzumab Deruxtecan Is Indicated For Treatment Of Adult Patients With Unresectable Or Metastatic Her2-Positive Breast Cancer Who Have Received A Prior Anti-Her2-Based Regimen; Locally Advanced Or Metastatic Her2-Positive Gastric Or Gastroesophageal Junction (Gej) Adenocarcinoma Who Have Received A Prior Anti-Her2- Based Regimen; Unresectable Or Metastatic Her2-Positive (Ihc3+) Solid Tumors Who Have Received Prior Systemic Treatment And Have No Satisfactory Alternative Treatment Options. 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As A Single Agent For Treatment Of Her2 Overexpressing Breast Cancer In Patients Who Have Received One Or More Chemotherapy Regimens For Metastatic Disease. Metastatic Gastric Cancer Is Indicated, In Combination With Cisplatin And Capecitabine Or 5fluorouracil, For The Treatment Of Patients With Her2 Overexpressing Metastatic Gastric Or Gastroesophageal Junction Adenocarcinoma Who Have Not Received Prior Treatment For Metastatic Disease.","dt_closure_dt":"05-DEC-2022","str_man_unit_name":"Mylan Laboratories Limited"},{"str_drug_name":"Trastuzumab Lyophilized Powder For Injection","str_composition":"Trastuzumab 150.0000 Milligram (Mg),L Histidine 2.1600 Milligram (Mg),L Histidine Hydrochloride 3.3600 Milligram (Mg),Polyethylene Glycol 33.6000 Milligram (Mg),D Sorbitol 115.2000 Milligram (Mg)","str_indication":"Adjuvant Breast Cancer Is Indicated For Adjuvant Treatment Of Her2 Overexpressing Node Positive Or Node Negative Er Pr Negative Or With One High Risk Feature, Metastatic Breast Cancer Is Indicated In Combination With Paclitaxel For First Line Treatment Of Her2 Overexpressing Metastatic Breast Cancer. As A Single Agent For Treatment Of Her2 Overexpressing Breast Cancer In Patients Who Have Received One Or More Chemotherapy Regimens For Metastatic Disease. Metastatic Gastric Cancer Is Indicated, In Combination With Cisplatin And Capecitabine Or 5fluorouracil, For The Treatment Of Patients With Her2 Overexpressing Metastatic Gastric Or Gastroesophageal Junction Adenocarcinoma Who Have Not Received Prior Treatment For Metastatic Disease.","dt_closure_dt":"05-DEC-2022","str_man_unit_name":"Mylan Laboratories Limited"},{"str_drug_name":"Trastuzumab Lyophilized Powder For Injection","str_composition":"Trastuzumab 420.0000 Milligram (Mg),L  Histidine 6.0000 Milligram (Mg),L  Histidine Hydrochloride 9.4000 Milligram (Mg),Polyethylene Glycol 94.1000 Milligram (Mg),D  Sorbitol 322.6000 Milligram (Mg)","str_indication":"Adjuvant Breast Cancer Is Indicated For Adjuvant Treatment Of Her2 Overexpressing Node Positive Or Node Negative Er Pr Negative Or With One High Risk Feature, Metastatic Breast Cancer Is Indicated In Combination With Paclitaxel For First Line Treatment Of Her2 Overexpressing Metastatic Breast Cancer. As A Single Agent For Treatment Of Her2 Overexpressing Breast Cancer In Patients Who Have Received One Or More Chemotherapy Regimens For Metastatic Disease. 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