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Benazepril Hydrochloride

NDC 65862-117 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078212
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBENAZEPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20080522
Marketing ended20261130
Package count1

External sources

Source: openFDA. Public-domain (CC0).