NDC 59651-202 – Fenofibrate

Fenofibrate 134 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC59651-202

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Aurobindo Pharma Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA212232
Marketed since
September 20, 2021
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
59651-202-01100 CAPSULE in 1 BOTTLE (59651-202-01)Sep 20, 2021

Other Fenofibrate products