Label: CITALOPRAM HYDROBROMIDE tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 51655-670-52 - Packager: Northwind Pharmaceuticals
- This is a repackaged label.
- Source NDC Code(s): 57664-509
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 3, 2014
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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
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INGREDIENTS AND APPEARANCE
CITALOPRAM HYDROBROMIDE
citalopram hydrobromide tabletProduct 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)