NDC 50090-6974 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-6974

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076509
Marketed since
June 22, 2022
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
50090-6974-090 TABLET in 1 BOTTLE (50090-6974-0)Dec 21, 2023

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