NDC 50090-7572 – Fenofibrate

Fenofibrate 54 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-7572

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216798
Marketed since
September 27, 2022
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 (2)

Package NDCDescriptionSince
50090-7572-090 TABLET, FILM COATED in 1 BOTTLE (50090-7572-0)Jun 5, 2025
50090-7572-130 TABLET, FILM COATED in 1 BOTTLE (50090-7572-1)Jun 5, 2025

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