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Benazepril Hydrochloride

NDC 68071-5028 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078212
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBENAZEPRIL HYDROCHLORIDE (40 mg/1)
Marketing started20080522
Package count1

External sources

Source: openFDA. Public-domain (CC0).