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Serving hundreds of leading biopharmaceutical companies globally:

Teva
Covington
Cantor Fitzgerald
Cipla
Cerilliant
Harvard Business School
Colorcon
McKinsey
Daiichi Sankyo

Generated: April 19, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 076251

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NDA 076251 describes FLUOXETINE HYDROCHLORIDE, which is a drug marketed by Barr, Dr Reddys Labs Ltd, Alembic Pharms Ltd, Ani Pharms Inc, Aurobindo Pharma, Carlsbad, Cr Double Crane, Heritage Pharms Inc, Ivax Sub Teva Pharms, Landela Pharm, Mylan, Mylan Pharms Inc, Par Pharm, Sandoz, Sciegen Pharms Inc, Specgx Llc, Sun Pharm Inds Ltd, Teva, Teva Pharms Usa, Wockhardt Ltd, Actavis Mid Atlantic, Apotex Inc, Aurobindo Pharma Ltd, Hi Tech Pharma, Lannett, Pharm Assoc, Silarx, Wockhardt Bio Ag, Alvogen, Dr Reddys Labs Inc, Fosun Pharma, Inventia Hlthcare, Par Form, Par Pharm Inc, and Torrent Pharms Ltd, and is included in forty-eight NDAs. It is available from seventy suppliers. Additional details are available on the FLUOXETINE HYDROCHLORIDE profile page.

The generic ingredient in FLUOXETINE HYDROCHLORIDE is fluoxetine hydrochloride. There are twenty-seven drug master file entries for this compound. Seventy-two suppliers are listed for this compound. Additional details are available on the fluoxetine hydrochloride profile page.
Summary for 076251
Tradename:FLUOXETINE HYDROCHLORIDE
Applicant:Barr
Ingredient:fluoxetine hydrochloride
Patents:0
Therapeutic Class:Antidepressants
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrengthEQ 40MG BASE
Approval Date:May 18, 2005TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

AstraZeneca
Queensland Health
US Army
Accenture
US Department of Justice
Mallinckrodt
Cipla
Daiichi Sankyo
McKinsey

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