FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 60505-3121 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA202252
Dosage form / routeCAPSULE · ORAL
Active ingredientsFENOFIBRATE (130 mg/1)
Marketing started20130726
Package count4

External sources

Source: openFDA. Public-domain (CC0).