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Serving hundreds of leading biopharmaceutical companies globally:

Colorcon
McKesson
Johnson and Johnson
Federal Trade Commission
Healthtrust
Citi
Chinese Patent Office
UBS
Covington

Generated: May 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 076204

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NDA 076204 describes MOEXIPRIL HYDROCHLORIDE, which is a drug marketed by Apotex Inc, Chartwell Rx, Glenmark Generics, Teva, Glenmark Pharms, and Heritage Pharms Inc, and is included in eight NDAs. It is available from five suppliers. Additional details are available on the MOEXIPRIL HYDROCHLORIDE profile page.

The generic ingredient in MOEXIPRIL HYDROCHLORIDE is hydrochlorothiazide; moexipril hydrochloride. There are thirty-two drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; moexipril hydrochloride profile page.
Summary for 076204
Tradename:MOEXIPRIL HYDROCHLORIDE
Applicant:Teva
Ingredient:moexipril hydrochloride
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details
Pharmacology for NDA: 076204
Suppliers and Packaging for NDA: 076204
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
MOEXIPRIL HYDROCHLORIDE moexipril hydrochloride TABLET;ORAL 076204 ANDA Teva Pharmaceuticals USA Inc 0093-0017 N 0093-0017-01
MOEXIPRIL HYDROCHLORIDE moexipril hydrochloride TABLET;ORAL 076204 ANDA Teva Pharmaceuticals USA Inc 0093-5150 N 0093-5150-01

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength7.5MG
Approval Date:May 8, 2003TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength15MG
Approval Date:May 8, 2003TE:ABRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Mallinckrodt
QuintilesIMS
Harvard Business School
Baxter
US Army
Healthtrust
Colorcon
Cipla
Medtronic

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