FDA NDC Directory · JSON-LD · Markdown

BENAZEPRIL HYDROCHLORIDE

NDC 72189-110 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA076118
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsBENAZEPRIL HYDROCHLORIDE (10 mg/1)
Marketing started20200612
Package count2

External sources

Source: openFDA. Public-domain (CC0).