NDC 71335-1286 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1286

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210138
Marketed since
July 20, 2018
Listing expires
December 31, 2027
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (5)

Package NDCDescriptionSince
71335-1286-130 TABLET in 1 BOTTLE (71335-1286-1)Sep 3, 2019
71335-1286-290 TABLET in 1 BOTTLE (71335-1286-2)Aug 28, 2019
71335-1286-360 TABLET in 1 BOTTLE (71335-1286-3)Dec 28, 2021
71335-1286-428 TABLET in 1 BOTTLE (71335-1286-4)Dec 28, 2021
71335-1286-5100 TABLET in 1 BOTTLE (71335-1286-5)Dec 28, 2021

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