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Benazepril Hydrochloride and Hydrochlorothiazide

NDC 68462-576 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA076631
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBENAZEPRIL HYDROCHLORIDE (5 mg/1)
HYDROCHLOROTHIAZIDE (6.25 mg/1)
Marketing started20150317
Package count1

External sources

Source: openFDA. Public-domain (CC0).