Home – Fenofibrate

Fenofibrate

FULL PRESCRIBING INFORMATION

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

Fenofibrate

Fenofibrate TABLET

Product Information
Product Type	Human prescription drug label	Item Code (Source)	NDC:51655-010(NDC:0093-2060)
Route of Administration	oral	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Fenofibrate FENOFIBRATE		145 mg

Product Characteristics
Color	Size	Imprint Code	Shape
white	18 mm	FO	OVAL

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	NDA021656	2014-05-20

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!