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Serving leading biopharmaceutical companies globally:

QuintilesIMS
Colorcon
Julphar
AstraZeneca
Mallinckrodt
Cipla
Accenture
Cerilliant
Federal Trade Commission
Medtronic

Generated: December 10, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 077476

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NDA 077476 describes RANITIDINE HYDROCHLORIDE, which is a drug marketed by Dr Reddys Labs Ltd, Mylan, Sandoz, Teva, Bedford, Mylan Labs Ltd, West-ward Pharms Int, Zydus Pharms Usa Inc, Actavis Mid Atlantic, Amneal Pharms, Apotex Inc, Aurobindo Pharma Ltd, Bio Pharm Inc, Breckenridge Pharm, Hi Tech Pharma, Nostrum Labs Inc, Pharm Assoc, Ranbaxy, Silarx, Taro, Tolmar, Vintage Pharms, Wockhardt, Amneal Pharms Ny, Apotex, Boehringer Ingelheim, Contract Pharmacal, Dr Reddys Labs Inc, Glenmark Pharms Inc, Ivax Sub Teva Pharms, Par Pharm, Perrigo, Perrigo R And D, Strides Pharma, Sun Pharm Inds Ltd, Watson Labs, and Watson Labs Inc, and is included in sixty-three NDAs. It is available from one hundred and thirty-two suppliers. Additional details are available on the RANITIDINE HYDROCHLORIDE profile page.

The generic ingredient in RANITIDINE HYDROCHLORIDE is ranitidine hydrochloride. There are forty-three drug master file entries for this compound. One hundred and thirty-nine suppliers are listed for this compound. Additional details are available on the ranitidine hydrochloride profile page.

Summary for 077476

Tradename:1
Applicant:1
Ingredient:1
Patents:0
Therapeutic Class:Gastrointestinal Agents
Formulation / Manufacturing:see details

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:SYRUP;ORALStrengthEQ 15MG BASE/ML
Approval Date:Jun 13, 2011TE:AARLD:No


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Serving leading biopharmaceutical companies globally:

US Army
Fuji
Daiichi Sankyo
Boehringer Ingelheim
Express Scripts
Fish and Richardson
Novartis
Covington
Chinese Patent Office
Merck

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