Celexa (Page 10 of 10)

Principal Display Panel – 10mg Bottle Label

NDC 0456-4010-01

Celexa ® citalopram HBr

Tablets-10 mg

Equivalent to 10 mg citalopram

100 Tablets

FOREST PHARMACEUTICALS, INC.
Subsidiary of Forest Laboratories, Inc. St. Louis, Missouri 63045

Principal Display Panel – 10mg Bottle Label
(click image for full-size original)

Principal Display Panel – 20mg Bottle Label

NDC 0456-4020-01

Celexa ® citalopram HBr

Tablets-20 mg

Equivalent to 20 mg citalopram

100 Tablets

FOREST PHARMACEUTICALS, INC.
Subsidiary of Forest Laboratories, Inc. St. Louis, Missouri 63045

Principal Display Panel – 20mg Bottle Label
(click image for full-size original)

Principal Display Panel – 40mg Bottle Label

NDC 0456-4040-01

Celexa ® citalopram HBr

Tablets-40 mg

Equivalent to 40 mg citalopram

100 Tablets

FOREST PHARMACEUTICALS, INC.
Subsidiary of Forest Laboratories, Inc. St. Louis, Missouri 63045

Principal Display Panel – 40mg Bottle Label
(click image for full-size original)
CELEXA citalopram hydrobromide tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0456-4010
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
copovidone
starch, corn
croscarmellose sodium
glycerin
lactose monohydrate
magnesium stearate
hypromelloses
cellulose, microcrystalline
polyethylene glycols
titanium dioxide
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
Product Characteristics
Color brown (beige) Score no score
Shape OVAL (Oval) Size 12mm
Flavor Imprint Code FP;10;MG
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0456-4010-01 100 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020822 07/17/1998
CELEXA citalopram hydrobromide tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0456-4020
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
citalopram hydrobromide (citalopram) citalopram 20 mg
Inactive Ingredients
Ingredient Name Strength
copovidone
starch, corn
croscarmellose sodium
glycerin
lactose monohydrate
magnesium stearate
hypromelloses
cellulose, microcrystalline
polyethylene glycols
titanium dioxide
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
Product Characteristics
Color pink (pink) Score 2 pieces
Shape OVAL (Oval) Size 12mm
Flavor Imprint Code F;P;20;MG
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0456-4020-01 100 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:0456-4020-63 10 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (0456-4020-11)
2 NDC:0456-4020-11 10 TABLET, FILM COATED in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (0456-4020-63)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020822 07/17/1998
CELEXA citalopram hydrobromide tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0456-4040
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
citalopram hydrobromide (citalopram) citalopram 40 mg
Inactive Ingredients
Ingredient Name Strength
copovidone
starch, corn
croscarmellose sodium
glycerin
lactose monohydrate
magnesium stearate
hypromelloses
cellulose, microcrystalline
polyethylene glycols
titanium dioxide
Product Characteristics
Color white (white) Score 2 pieces
Shape OVAL (Oval) Size 12mm
Flavor Imprint Code F;P;40;MG
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0456-4040-01 100 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:0456-4040-63 10 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (0456-4040-11)
2 NDC:0456-4040-11 10 TABLET, FILM COATED in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (0456-4040-63)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020822 07/17/1998
Labeler — Forest Laboratories, Inc. (001288281)
Establishment
Name Address ID/FEI Operations
Forest Pharmaceuticals, Inc 139645477 PACK (0456-4010), PACK (0456-4020), PACK (0456-4040)
Establishment
Name Address ID/FEI Operations
H. Lundbeck A/S 310613542 API MANUFACTURE (0456-4010), API MANUFACTURE (0456-4020), API MANUFACTURE (0456-4040)

Revised: 07/2014 Forest Laboratories, Inc.

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