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McKesson
Express Scripts
Fuji
Dow
Cantor Fitzgerald
Queensland Health
Daiichi Sankyo
Farmers Insurance
Mallinckrodt

Generated: June 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 090096

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NDA 090096 describes MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE, which is a drug marketed by Chartwell Rx, Glenmark Pharms, Heritage Pharms Inc, and Teva, and is included in four NDAs. It is available from four suppliers. Additional details are available on the MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE profile page.

The generic ingredient in MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 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 090096

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength12.5MG;7.5MG
Approval Date:Sep 25, 2008TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength12.5MG;15MG
Approval Date:Sep 25, 2008TE:RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength25MG;15MG
Approval Date:Sep 25, 2008TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Chinese Patent Office
UBS
McKinsey
Healthtrust
Argus Health
US Army
US Department of Justice
Cipla
Fuji

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