NDC 59651-575 – Fenofibrate

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

Human Prescription Drug

Product NDC59651-575

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Aurobindo Pharma Limited
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 (1)

Package NDCDescriptionSince
59651-575-9090 TABLET, FILM COATED in 1 BOTTLE (59651-575-90)Sep 27, 2022

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