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Serving hundreds of leading biopharmaceutical companies globally:

Harvard Business School
US Department of Justice
Daiichi Sankyo

Generated: March 24, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 072688

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NDA 072688 describes AMOXAPINE, which is a drug marketed by Upsher-smith Labs, Watson Labs, and Watson Pharms Teva, and is included in twelve NDAs. It is available from four suppliers. Additional details are available on the AMOXAPINE profile page.

The generic ingredient in AMOXAPINE is amoxapine. There are four drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the amoxapine profile page.
Summary for 072688
Applicant:Watson Labs
Therapeutic Class:Antidepressants
Formulation / Manufacturing:see details
Suppliers and Packaging for NDA: 072688
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
AMOXAPINE amoxapine TABLET;ORAL 072688 ANDA Actavis Pharma, Inc. 0591-5713 N 0591-5713-01
AMOXAPINE amoxapine TABLET;ORAL 072688 ANDA Cardinal Health 55154-5393 E 55154-5393-0

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength25MG
Approval Date:Aug 28, 1992TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

US Department of Justice
Daiichi Sankyo
US Army

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