CITALOPRAM HYDROBROMIDE tablet

CITALOPRAM HYDROBROMIDE by

Drug Labeling and Warnings

CITALOPRAM HYDROBROMIDE 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: 51655-670-52

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

WARNINGS AND PRECAUTIONS

INGREDIENTS AND APPEARANCE

CITALOPRAM HYDROBROMIDE 
citalopram hydrobromide tablet

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 51655-670(NDC:57664-509)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CITALOPRAM HYDROBROMIDE (UNII: I1E9D14F36) (CITALOPRAM - UNII:0DHU5B8D6V)	CITALOPRAM	40 mg  in 30

Product Characteristics
Color	white	Score	no score
Shape	OVAL	Size	13mm
Flavor		Imprint Code	509
Contains

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	04/03/2014

Labeler - Northwind Pharmaceuticals (036986393)

Registrant - Northwind Pharmaceuticals (036986393)

Establishment
Name	Address	ID/FEI	Business Operations
Northwind Pharmaceuticals		036986393	repack(51655-670)