FDA NDC Directory · JSON-LD · Markdown

FENOFIBRIC ACID

NDC 69315-282 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211626
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsFENOFIBRIC ACID (135 mg/1)
Marketing started20190718
Package count1

External sources

Source: openFDA. Public-domain (CC0).