NDC 70518-4721 – Fenofibrate

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

Human Prescription Drug

Product NDC70518-4721

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216798
Marketed since
August 4, 2026
Listing expires
December 31, 2027
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (1)

Package NDCDescriptionSince
70518-4721-090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4721-0)Aug 4, 2026

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