NDC 31722-595 – Fenofibrate

Fenofibrate 48 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC31722-595

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204598
Marketed since
July 14, 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 (4)

Package NDCDescriptionSince
31722-595-3030 TABLET, FILM COATED in 1 BOTTLE (31722-595-30)Jul 14, 2016
31722-595-31100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-31)Jul 14, 2016
31722-595-32100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-32)Jul 14, 2016
31722-595-9090 TABLET, FILM COATED in 1 BOTTLE (31722-595-90)Jul 14, 2016

Recalls mentioning this NDC

Other Fenofibrate products