NDC 71335-2654 – Fenofibrate

Fenofibrate 48 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2654

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204598
Marketed since
July 14, 2016
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 (3)

Package NDCDescriptionSince
71335-2654-130 TABLET, FILM COATED in 1 BOTTLE (71335-2654-1)Jun 20, 2025
71335-2654-290 TABLET, FILM COATED in 1 BOTTLE (71335-2654-2)Jun 20, 2025
71335-2654-328 TABLET, FILM COATED in 1 BOTTLE (71335-2654-3)Jun 20, 2025

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