FDA NDC Directory · JSON-LD · Markdown

fenofibrate

NDC 55700-876 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerQuality Care Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210138
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20200721
Marketing ended20270630
Package count1

External sources

Source: openFDA. Public-domain (CC0).