FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 70518-4326 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA076509
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20250410
Package count1

External sources

Source: openFDA. Public-domain (CC0).