Home – fluoxetine hydrochloride

fluoxetine hydrochloride

FULL PRESCRIBING INFORMATION

NDC: 51655-100-52

MFG: 65862-193-99

Fluoxetine Capsules

20 MG

30 Tablets

Rx Only

Lot# NW60950001

Exp. Date: 12/2016

Each capsule contains: Fluoxetine hydrochloride USP equivalent to 20 mg of fluoxetine

Dosage: See package insert

Store at 68 to 77 degrees F.

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

Mfg. by: Aurobindo Pharma Ltd, India for

Aurobindo Pharma Inc. NJ, USA

Lot# FX2014013-A exp. 12/2016

Repackaged by: Northwind Pharmaceuticals, Indianapolis, IN 46256

fluoxetine hydrochloride

fluoxetine hydrochloride CAPSULE

Product Information
Product Type	Human prescription drug label	Item Code (Source)	NDC:51655-100(NDC:65862-193)
Route of Administration	oral	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FLUOXETINE HYDROCHLORIDE FLUOXETINE		20 mg

Product Characteristics
Color	Size	Imprint Code	Shape
white	16 mm	E91	capsule

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:51655-100-52	30 in 1 BOTTLE, DISPENSING

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA078619	2014-05-20

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!