FDA NDC Directory · JSON-LD · Markdown

FENOFIBRATE

NDC 0615-8530 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA208709
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (145 mg/1)
Marketing started20161215
Package count1

External sources

Source: openFDA. Public-domain (CC0).