NDC 71335-2628 – Fenofibrate

Fenofibrate 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2628

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217732
Marketed since
September 7, 2023
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (1)

Package NDCDescriptionSince
71335-2628-190 TABLET in 1 BOTTLE (71335-2628-1)Apr 14, 2025

Other Fenofibrate products