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Alfuzosin Hydrochloride

NDC 51655-087 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079060
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsALFUZOSIN HYDROCHLORIDE (10 mg/1)
Marketing started20221004
Package count1

External sources

Source: openFDA. Public-domain (CC0).