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Benazepril Hydrochloride

NDC 70518-4633 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA076267
Dosage form / routeTABLET · ORAL
Active ingredientsBENAZEPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20260425
Package count1

External sources

Source: openFDA. Public-domain (CC0).