FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 35561-343 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBostal LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207803
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFENOFIBRATE (54 mg/1)
Marketing started20190630
Package count3

External sources

Source: openFDA. Public-domain (CC0).