NDC 60687-853 – Fenofibrate

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

Human Prescription Drug

Product NDC60687-853

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076433
Marketed since
April 19, 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
60687-853-2130 BLISTER PACK in 1 CARTON (60687-853-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-853-11)Apr 19, 2025

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