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Generated: December 12, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 077144

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NDA 077144 describes FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE, which is a drug marketed by Actavis Labs Fl Inc, Aurobindo Pharma, Emcure Pharms India, Invagen Pharms, Mylan, Sandoz, Sun Pharm Inds Ltd, Teva, and Watson Labs, and is included in nine NDAs. It is available from eight suppliers. Additional details are available on the FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE profile page.

The generic ingredient in FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE is fosinopril sodium; hydrochlorothiazide. There are six drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the fosinopril sodium; hydrochlorothiazide profile page.

Summary for 077144

Tradename:1
Applicant:1
Ingredient:1
Patents:0
Formulation / Manufacturing:see details

Summary for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength10MG;12.5MG
Approval Date:Aug 16, 2005TE:RLD:No

Summary for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength20MG;12.5MG
Approval Date:Aug 16, 2005TE:RLD:No


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Serving leading biopharmaceutical companies globally:

Julphar
McKesson
Daiichi Sankyo
Harvard Business School
Boehringer Ingelheim
Teva
Fish and Richardson
Argus Health
AstraZeneca
Federal Trade Commission

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