Home – Fenofibrate

Fenofibrate

FULL PRESCRIBING INFORMATION

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

Fenofibrate TABLET

Product Information
Product Type	Human prescription drug label	Item Code (Source)	NDC:51655-009(NDC:0115-5522)
Route of Administration	oral	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Fenofibrate FENOFIBRATE		160 mg

Product Characteristics
Color	Size	Imprint Code	Shape
white	15 mm	G;352	OVAL

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	2014-05-07

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!