BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE Detail

Drug Name(s):
BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

FDA Application No.:
NDA 076612

Active Ingredient(s):
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Company:
GENPHARM

Products on Application NDA 076612:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	10MG;12.5MG	TABLET; ORAL	Prescription	AB
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE	20MG;25MG	TABLET; ORAL	Prescription	AB

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last updated on 12-05-2008

BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE Detail

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