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FENOFIBRIC ACID DELAYED-RELEASE

NDC 42385-945 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic nameFenofibric Acid
Labeler / ManufacturerLaurus Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211626
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsFENOFIBRIC ACID (135 mg/1)
Marketing started20200824
Package count3

External sources

Source: openFDA. Public-domain (CC0).