FDA NDC Directory · JSON-LD · Markdown

Benazepril Hydrochloride

NDC 62559-526 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076333
Dosage form / routeTABLET · ORAL
Active ingredientsBENAZEPRIL HYDROCHLORIDE (20 mg/1)
Marketing started20260727
Package count2

External sources

Source: openFDA. Public-domain (CC0).