FDA NDC Directory · JSON-LD · Markdown

fenofibrate

NDC 0615-8270 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA210138
Dosage form / routeTABLET · ORAL
Active ingredientsFENOFIBRATE (160 mg/1)
Marketing started20180720
Package count1

External sources

Source: openFDA. Public-domain (CC0).