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Serving hundreds of leading biopharmaceutical companies globally:

Baxter
Boehringer Ingelheim
Mallinckrodt
US Army
Colorcon
Medtronic
Cerilliant
Johnson and Johnson
Express Scripts

Generated: August 20, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 076866

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NDA 076866 describes OLANZAPINE, which is a drug marketed by Luitpold, Sandoz Inc, Ajanta Pharma Ltd, Apotex Inc, Aurobindo Pharma Ltd, Barr Labs Inc, Dr Reddys Labs Ltd, Hec Pharm, Invagen Pharms, Jubilant Generics, Macleods Pharms Ltd, Mylan Pharms Inc, Orchid Hlthcare, Par Pharm, Sun Pharm Inds, Torrent Pharms Llc, Alkem Labs Ltd, Hikma Pharms, Ivax Pharms Inc, Qilu Pharm Co Ltd, Teva Pharms, Torrent Pharms Ltd, Zydus Pharms Usa Inc, and Sandoz, and is included in thirty-seven NDAs. It is available from thirty-nine suppliers. Additional details are available on the OLANZAPINE profile page.

The generic ingredient in OLANZAPINE is fluoxetine hydrochloride; olanzapine. There are twenty-seven drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the fluoxetine hydrochloride; olanzapine profile page.
Summary for 076866
Tradename:OLANZAPINE
Applicant:Mylan Pharms Inc
Ingredient:olanzapine
Patents:0
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength2.5MG
Approval Date:Apr 23, 2012TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength5MG
Approval Date:Apr 23, 2012TE:RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength7.5MG
Approval Date:Apr 23, 2012TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

AstraZeneca
Merck
Federal Trade Commission
US Department of Justice
Harvard Business School
McKesson
QuintilesIMS
Johnson and Johnson
Chubb

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