FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 50268-338 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA090856
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (48 mg/1)
Marketing started20220922
Package count1

External sources

Source: openFDA. Public-domain (CC0).