NDC 62332-350 – Fenofibrate

Fenofibrate 54 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC62332-350

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213252
Marketed since
January 23, 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 (3)

Package NDCDescriptionSince
62332-350-3030 TABLET, FILM COATED in 1 BOTTLE (62332-350-30)Jan 23, 2020
62332-350-71500 TABLET, FILM COATED in 1 BOTTLE (62332-350-71)Jan 23, 2020
62332-350-9090 TABLET, FILM COATED in 1 BOTTLE (62332-350-90)Jan 23, 2020

Other Fenofibrate products