FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 35561-249 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBostal LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208476
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFENOFIBRATE (48 mg/1)
Marketing started20210101
Package count4

External sources

Source: openFDA. Public-domain (CC0).