NDC 50090-5854 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-5854

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204019
Marketed since
July 1, 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 (2)

Package NDCDescriptionSince
50090-5854-030 TABLET in 1 BOTTLE (50090-5854-0)Nov 11, 2021
50090-5854-190 TABLET in 1 BOTTLE (50090-5854-1)Nov 11, 2021

Other Fenofibrate products