NDC 82619-101 – Fenofibrate

Fenofibrate 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82619-101

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Creekwood Pharmaceuticals LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217732
Marketed since
September 7, 2023
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
82619-101-0190 TABLET in 1 BOTTLE (82619-101-01)Sep 20, 2023

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