FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 72162-2170 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameFENOFIBRATE
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA210670
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20200131
Package count1

External sources

Source: openFDA. Public-domain (CC0).