NDC 0904-7539 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0904-7539

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Major Pharmaceuticals
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213864
Marketed since
May 22, 2025
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
0904-7539-0430 BLISTER PACK in 1 CARTON (0904-7539-04) / 1 TABLET in 1 BLISTER PACKMay 22, 2025

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