FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 62332-360 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210476
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFENOFIBRATE (48 mg/1)
Marketing started20190809
Package count3

External sources

Source: openFDA. Public-domain (CC0).