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PRINCIPAL DISPLAY PANEL
NDC: 51655-009-52
MFG: 0115-552-10
Fenofibrate 160mg
30 Tablets
Rx Only
Lot# NW89560001
Exp Date: 09/2015
Each tablet contains: 160mg of fenofibrate
Dosage: See package insert
Store at 60-77 degrees F. Store in a tight, light-resistant container (See USP)
Keep out of the reach of children.
Dist. By: Global Pharmaceuticals
Division of IMPAX Laboratories, Inc
Philadelphia, PA 19124 USA
Product of Taiwan Lot: 10008621
Repackaged by Northwind Pharmaceuticals, Indianapolis, IN 46256
- WARNINGS AND PRECAUTIONS
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INGREDIENTS AND APPEARANCE
FENOFIBRATE
fenofibrate tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-009(NDC:0115-5522) Route of Administration oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FENOFIBRATE (UNII: U202363UOS) (FENOFIBRATE - UNII:U202363UOS) FENOFIBRATE 160 mg in 30 Product Characteristics Color white Score no score Shape OVAL Size 15mm Flavor Imprint Code G;352 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51655-009-52 30 in 1 BOTTLE, DISPENSING Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076509 05/07/2014 Labeler - Northwind Pharmaceuticals (036986393) Registrant - Northwind Pharmaceuticals (036986393) Establishment Name Address ID/FEI Business Operations Northwind Pharmaceuticals 036986393 repack(51655-009)