NDC 0378-3066 – Fenofibrate

Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0378-3066

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202856
Marketed since
May 14, 2013
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 (2)

Package NDCDescriptionSince
0378-3066-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3066-05)May 14, 2013
0378-3066-7790 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3066-77)May 14, 2013

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