FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 43975-306 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209504
Dosage form / routeCAPSULE · ORAL
Active ingredientsFENOFIBRATE (200 mg/1)
Marketing started20180501
Package count2

External sources

Source: openFDA. Public-domain (CC0).