FDA NDC Directory · JSON-LD · Markdown

Alfuzosin Hydrochloride

NDC 72162-1449 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA079057
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsALFUZOSIN HYDROCHLORIDE (10 mg/1)
Marketing started20111122
Package count1

External sources

Source: openFDA. Public-domain (CC0).