Citalopram Hydrobromide (Page 9 of 9)

CITALOPRAM HYDROBROMIDE TABLET

Label Image
(click image for full-size original)
CITALOPRAM HYDROBROMIDE citalopram hydrobromide tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:64725-0507(NDC:57664-507)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CITALOPRAM HYDROBROMIDE (CITALOPRAM) CITALOPRAM 10 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
CELLULOSE, MICROCRYSTALLINE
STARCH, CORN
COPOVIDONE K25-31
CROSCARMELLOSE SODIUM
SILICON DIOXIDE
MAGNESIUM STEARATE
TITANIUM DIOXIDE
POLYETHYLENE GLYCOL 4000
HYPROMELLOSE 2910 (6 MPA.S)
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
Product Characteristics
Color PINK (PEACH) Score no score
Shape ROUND Size 6mm
Flavor Imprint Code c
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:64725-0507-1 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077032 11/12/2004
Labeler — TYA Pharmaceuticals (938389038)
Registrant — TYA Pharmaceuticals (938389038)
Establishment
Name Address ID/FEI Operations
TYA Pharmaceuticals 938389038 RELABEL (64725-0507), REPACK (64725-0507)

Revised: 01/2013 TYA Pharmaceuticals

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