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Alfuzosin Hydrochloride

NDC 84386-153 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA079060
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsALFUZOSIN HYDROCHLORIDE (10 mg/1)
Marketing started20260701
Package count5

External sources

Source: openFDA. Public-domain (CC0).