FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 42385-935 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLaurus Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA210606
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFENOFIBRATE (54 mg/1)
Marketing started20200113
Package count4

External sources

Source: openFDA. Public-domain (CC0).