NDC 27241-117 – Fenofibrate

Fenofibrate 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC27241-117

Product details

Brand name
Fenofibrate
Generic name
Fenofibrate
Labeler
Ajanta Pharma USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210138
Marketed since
July 20, 2018
Listing expires
December 31, 2027
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fenofibrate →

Package NDC codes (2)

Package NDCDescriptionSince
27241-117-0390 TABLET in 1 BOTTLE (27241-117-03)Jul 20, 2018
27241-117-05500 TABLET in 1 BOTTLE (27241-117-05)Jul 20, 2018

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