FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 69238-1262 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209950
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (54 mg/1)
Marketing started20180323
Package count1

External sources

Source: openFDA. Public-domain (CC0).