NDC 72603-841 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72603-841

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
NorthStar RxLLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213864
Marketed since
September 29, 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 (2)

Package NDCDescriptionSince
72603-841-0190 TABLET in 1 BOTTLE (72603-841-01)Sep 29, 2025
72603-841-02500 TABLET in 1 BOTTLE (72603-841-02)Sep 29, 2025

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