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fenofibrate

NDC 42385-950 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLaurus Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211122
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (48 mg/1)
Marketing started20200318
Package count3

External sources

Source: openFDA. Public-domain (CC0).