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Fenofibrate

NDC 62332-350 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213252
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFENOFIBRATE (54 mg/1)
Marketing started20200123
Package count3

External sources

Source: openFDA. Public-domain (CC0).