NDC 50090-5796 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-5796

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200884
Marketed since
June 1, 2018
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 (1)

Package NDCDescriptionSince
50090-5796-090 TABLET, FILM COATED in 1 BOTTLE (50090-5796-0)Oct 13, 2021

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