Home – CITALOPRAM HYDROBROMIDE

CITALOPRAM HYDROBROMIDE

FULL PRESCRIBING INFORMATION

NDC: 51655-670-52

MFG: 57664-509-13

Citalopram 40 MG

30 TABLETS

RX ONLY

Dosage: See package insert

Store at 68 to 77 degrees F.

Keep out of reach of children.

Each tablet contains Citalopram hydrobromide, UPS equivalent to 40mg citalopram base

Mfg by: Sun Pharmaceutical Ind. Ltd Halol-Baroda Highway, Halol-389 350, Gujarat, India

Distributed by Caraco Pharmaceuticals Laboratories, Ltd, 1150 Elijah McCoy Drive, Detroit, MI 48202

Batch # JKM4285A

Repackaged by Northwind Pharmaceuticals Indianapolis, IN 46256

Lot # NW89530001 EXP Date: 10/2015

CITALOPRAM HYDROBROMIDE

CITALOPRAM HYDROBROMIDE TABLET

Product Information
Product Type	Human prescription drug label	Item Code (Source)	NDC:51655-670(NDC:57664-509)
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
citalopram hydrobromide CITALOPRAM		40 mg

Product Characteristics
Color	Size	Imprint Code	Shape
white	13 mm	509	OVAL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:51655-670-52	30 in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA077032	2014-04-03

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!