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Benazepril Hydrochloride

NDC 68071-1969 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076118
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsBENAZEPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20140101
Package count4

External sources

Source: openFDA. Public-domain (CC0).