NDC 42385-936 – Fenofibrate

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

Human Prescription Drug

Product NDC42385-936

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Laurus Labs Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210606
Marketed since
January 13, 2020
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 (4)

Package NDCDescriptionSince
42385-936-05500 TABLET, FILM COATED in 1 BOTTLE (42385-936-05)Jan 13, 2020
42385-936-111000 TABLET, FILM COATED in 1 BOTTLE (42385-936-11)Jan 13, 2020
42385-936-3030 TABLET, FILM COATED in 1 BOTTLE (42385-936-30)Jan 13, 2020
42385-936-9090 TABLET, FILM COATED in 1 BOTTLE (42385-936-90)Jan 13, 2020

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