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Fenofibrate

NDC 48433-040 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namefenofibrate
Labeler / ManufacturerSafecor Health, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202856
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFENOFIBRATE (145 mg/1)
Marketing started20260317
Package count1

External sources

Source: openFDA. Public-domain (CC0).