CITALOPRAM HYDROBROMIDE description, usages, side effects, indications, overdosage, supplying and lots more!

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CITALOPRAM HYDROBROMIDE

Northwind Pharmaceuticals
Northwind Pharmaceuticals




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

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


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