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Fenofibrate

NDC 69315-290 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210606
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20220820
Package count2

External sources

Source: openFDA. Public-domain (CC0).