FDA NDC Directory · JSON-LD · Markdown

Fenofibrate

NDC 42858-134 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerRhodes Pharmaceuticals L.P.
Marketing categoryAbbreviated NDA (generic) · App ANDA075753
Dosage form / routeCAPSULE · ORAL
Active ingredientsFENOFIBRATE (134 mg/1)
Marketing started20170601
Package count1

External sources

Source: openFDA. Public-domain (CC0).