NDC 71335-1701 – Fenofibrate

Fenofibrate 48 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71335-1701

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA205118
Marketed since
May 5, 2016
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 (3)

Package NDCDescriptionSince
71335-1701-130 TABLET, COATED in 1 BOTTLE (71335-1701-1)Jan 12, 2021
71335-1701-290 TABLET, COATED in 1 BOTTLE (71335-1701-2)Sep 8, 2020
71335-1701-328 TABLET, COATED in 1 BOTTLE (71335-1701-3)Dec 29, 2021

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