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Serving leading biopharmaceutical companies globally:

Johnson and Johnson
Farmers Insurance
Harvard Business School
Merck
Daiichi Sankyo
Mallinckrodt
Medtronic
AstraZeneca
US Department of Justice
Queensland Health

Generated: February 17, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 201741

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NDA 201741 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, 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, and Sandoz, and is included in thirty-five NDAs. It is available from thirty-eight 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 201741
Tradename:OLANZAPINE
Applicant:Luitpold
Ingredient:olanzapine
Patents:0
Therapeutic Class:Antipsychotics
Bipolar Agents
Formulation / Manufacturing:see details
Pharmacology for NDA: 201741
Suppliers and Packaging for NDA: 201741
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
OLANZAPINE olanzapine INJECTABLE;INTRAMUSCULAR 201741 ANDA American Regent, Inc. 0517-0955 N 0517-0955-01
OLANZAPINE olanzapine INJECTABLE;INTRAMUSCULAR 201741 ANDA TYA Pharmaceuticals 64725-0955 E 64725-0955-1

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INTRAMUSCULARStrength10MG/VIAL
Approval Date:Mar 20, 2012TE:APRLD:No

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Cantor Fitzgerald
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Express Scripts
Dow
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Chubb
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US Army
Accenture

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