FDA NDC Directory · JSON-LD · Markdown

fenofibrate

NDC 62135-899 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerChartwell RX, LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA211407
Dosage form / routeCAPSULE · ORAL
Active ingredientsFENOFIBRATE (200 mg/1)
Marketing started20240131
Package count1

External sources

Source: openFDA. Public-domain (CC0).