FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 71205-666 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA213864
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (54 mg/1)
Marketing started20200910
Package count3

External sources

Source: openFDA. Public-domain (CC0).