NDC 59651-201 – Fenofibrate

Fenofibrate 67 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC59651-201

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
59651-201-01100 CAPSULE in 1 BOTTLE (59651-201-01)Sep 20, 2021

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