NDC 0115-5511 – Fenofibrate

Fenofibrate 54 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0115-5511

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076509
Marketed since
February 1, 2010
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 (4)

Package NDCDescriptionSince
0115-5511-01100 TABLET in 1 BOTTLE (0115-5511-01)Feb 1, 2010
0115-5511-02500 TABLET in 1 BOTTLE (0115-5511-02)Feb 1, 2010
0115-5511-031000 TABLET in 1 BOTTLE (0115-5511-03)Feb 1, 2010
0115-5511-1090 TABLET in 1 BOTTLE (0115-5511-10)Feb 1, 2010

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