NDC 69315-282 – Fenofibric Acid

Fenofibric Acid 135 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC69315-282

Product details

Brand name
Fenofibric Acid
Generic name
Fenofibric Acid
Labeler
Leading Pharma, LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA211626
Marketed since
July 18, 2019
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibric acid →

Package NDC codes (1)

Package NDCDescriptionSince
69315-282-0990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (69315-282-09)Jul 18, 2019

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