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: 51655-010-52

MFG: 0093-2060-98

Fenofibrate 145mg

30 Tablets

Rx only

Lot# NW89520001

Exp Date: 06/2016

Each tablet contains: 145mg of fenofibrate

Dosage: See package insert

Store at 77 degrees F. Protect from moisture.

Store in a tight, light-resistant container (See USP) Keep out of reach of children.

Mfg by: Fournier Laboratories Ireland Limited Anngrove, Carrigtwohill Co. Cork, Ireland

Mfg for: Teva Pharmaceuticals USA Sellersville, PA 18960 Lot: 1007225

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: 51655-010(NDC:0093-2060)
Route of Administration	oral

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FENOFIBRATE (UNII: U202363UOS) (FENOFIBRATE - UNII:U202363UOS)	FENOFIBRATE	145 mg  in 30

Product Characteristics
Color	white	Score	no score
Shape	OVAL	Size	18mm
Flavor		Imprint Code	FO
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51655-010-52	30 in 1 BOTTLE, DISPENSING

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA authorized generic	NDA021656	05/20/2014

Labeler - Northwind Pharmaceuticals (036986393)

Registrant - Northwind Pharmaceuticals (036986393)

Establishment
Name	Address	ID/FEI	Business Operations
Northwind Pharmaceuticals		036986393	repack(51655-010)