CITALOPRAM HYDROBROMIDE- citalopram hydrobromide tablet 
Northwind Pharmaceuticals

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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 40

CITALOPRAM HYDROBROMIDE 
citalopram hydrobromide tablet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:51655-670(NDC:57664-509)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CITALOPRAM HYDROBROMIDE (UNII: I1E9D14F36) (CITALOPRAM - UNII:0DHU5B8D6V) CITALOPRAM40 mg  in 30 
Product Characteristics
ColorwhiteScoreno score
ShapeOVALSize13mm
FlavorImprint Code 509
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51655-670-5230 in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07703204/03/2014
Labeler - Northwind Pharmaceuticals (036986393)
Registrant - Northwind Pharmaceuticals (036986393)
Establishment
NameAddressID/FEIBusiness Operations
Northwind Pharmaceuticals036986393repack(51655-670)

Revised: 4/2014
Document Id: 7bdada38-7f1e-4e26-9585-195d1bfb1a57
Set id: 43f42e63-8b70-429a-93ce-a35bb2e74a6c
Version: 1
Effective Time: 20140403
 
Northwind Pharmaceuticals