NDC 0378-4391 – Fenofibrate

Fenofibrate 120 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0378-4391

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204475
Marketed since
June 23, 2016
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
0378-4391-7790 TABLET in 1 BOTTLE, PLASTIC (0378-4391-77)Jun 23, 2016

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