FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 72603-841 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213864
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20250929
Package count2

External sources

Source: openFDA. Public-domain (CC0).