FENOFIBRATE by Northwind Pharmaceuticals FENOFIBRATE tablet

FENOFIBRATE by

Drug Labeling and Warnings

FENOFIBRATE by is a Prescription medication manufactured, distributed, or labeled by Northwind Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

FENOFIBRATE 
fenofibrate tablet

Product 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)