FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 71335-2628 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefenofibrate
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA217732
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (40 mg/1)
Marketing started20230907
Package count1

External sources

Source: openFDA. Public-domain (CC0).