NDC 71335-3086 – Fenofibrate

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

Human Prescription Drug

Product NDC71335-3086

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216798
Marketed since
September 27, 2022
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
71335-3086-130 TABLET, FILM COATED in 1 BOTTLE (71335-3086-1)Feb 16, 2026
71335-3086-290 TABLET, FILM COATED in 1 BOTTLE (71335-3086-2)Feb 16, 2026
71335-3086-360 TABLET, FILM COATED in 1 BOTTLE (71335-3086-3)Feb 16, 2026
71335-3086-428 TABLET, FILM COATED in 1 BOTTLE (71335-3086-4)Feb 16, 2026
71335-3086-5100 TABLET, FILM COATED in 1 BOTTLE (71335-3086-5)Feb 16, 2026

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