FENOFIBRATE- fenofibrate tablet 
Northwind Pharmaceuticals

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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

Fenofibrate 51655-009

FENOFIBRATE 
fenofibrate tablet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:51655-009(NDC:0115-5522)
Route of Administrationoral
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FENOFIBRATE (UNII: U202363UOS) (FENOFIBRATE - UNII:U202363UOS) FENOFIBRATE160 mg  in 30 
Product Characteristics
ColorwhiteScoreno score
ShapeOVALSize15mm
FlavorImprint Code G;352
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51655-009-5230 in 1 BOTTLE, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07650905/07/2014
Labeler - Northwind Pharmaceuticals (036986393)
Registrant - Northwind Pharmaceuticals (036986393)
Establishment
NameAddressID/FEIBusiness Operations
Northwind Pharmaceuticals036986393repack(51655-009)

Revised: 5/2014
Document Id: 7e1779df-a430-4654-80fc-95cf391c279d
Set id: 4b4447a1-8136-4258-b2c8-c5f9c1bcec92
Version: 1
Effective Time: 20140507
 
Northwind Pharmaceuticals