NDC 71335-0741 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0741

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076433
Marketed since
June 1, 2017
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 (5)

Package NDCDescriptionSince
71335-0741-130 TABLET, FILM COATED in 1 BOTTLE (71335-0741-1)Mar 16, 2018
71335-0741-290 TABLET, FILM COATED in 1 BOTTLE (71335-0741-2)Mar 16, 2018
71335-0741-360 TABLET, FILM COATED in 1 BOTTLE (71335-0741-3)Dec 27, 2021
71335-0741-428 TABLET, FILM COATED in 1 BOTTLE (71335-0741-4)Dec 27, 2021
71335-0741-5100 TABLET, FILM COATED in 1 BOTTLE (71335-0741-5)Dec 27, 2021

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