Prescription Drug Information: Citalopram (Page 7 of 7)

PACKAGE/LABEL DISPLAY PANEL – Carton – 10 mg

10 mg Citalopram Tablets Carton
(click image for full-size original)

NDC 68084- 737 -01

Citalopram
Tablets, USP

10 mg

100 Tablets (10 x 10)               Rx Only

PHARMACIST: Dispense with the accompanying Medication
Guide to each patient.

Each Tablet Contains:
Citalopram hydrobromide USP equivalent to 10 mg citalopram base.

Usual Dosage: See package insert for full prescribing information.

Store at 20° to 25°C (68° to 77°F); excursions permitted between 15°
to 30°C (59° to 86°F) [see USP Controlled Room Temperature].

Keep this and all drugs out of reach of children.

FOR YOUR PROTECTION: Do not use if blister is torn or broken.

The drug product contained in this package is from
NDC # 65862-005, Aurobindo Pharma USA, Inc.

Packaged and Distributed by:
American Health Packaging
Columbus, Ohio 43217

073701 0273701/0419

PACKAGE/LABEL DISPLAY PANEL – Blister – 10 mg

10 mg Citalopram Tablet Blister
(click image for full-size original)

Citalopram Tablet, USP

10 mg

PACKAGE/LABEL DISPLAY PANEL – Carton – 20 mg

20 mg Citalopram Tablets Carton
(click image for full-size original)

NDC 68084- 744 -01

Citalopram
Tablets, USP

20 mg

100 Tablets (10 x 10)               Rx Only

PHARMACIST: Dispense with the accompanying Medication
Guide to each patient.

Each Tablet Contains:
Citalopram hydrobromide USP equivalent to 20 mg citalopram base.

Usual Dosage: See package insert for full prescribing information.

Store at 20° to 25°C (68° to 77°F); excursions permitted between
15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature].

Keep this and all drugs out of reach of children.

FOR YOUR PROTECTION: Do not use if blister is torn or broken.

The drug product contained in this package is from
NDC # 65862-006, Aurobindo Pharma USA, Inc.

Packaged and Distributed by:
American Health Packaging
Columbus, Ohio 43217

074401 0274401/0319

PACKAGE/LABEL DISPLAY PANEL – Blister – 20 mg

20 mg Citalopram Tablet Blister
(click image for full-size original)

Citalopram Tablet, USP

20 mg

CITALOPRAM citalopram hydrobromide tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68084-737(NDC:65862-005)
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 K25-31
STARCH, CORN
CROSCARMELLOSE SODIUM
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
HYPROMELLOSE 2910 (6 MPA.S)
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL 400
TITANIUM DIOXIDE
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
Product Characteristics
Color orange (Peach) Score no score
Shape ROUND (Biconvex) Size 5mm
Flavor Imprint Code A;05
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68084-737-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (68084-737-11)
1 NDC:68084-737-11 1 TABLET, FILM COATED in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (68084-737-01)
Image of Product
(click image for full-size original)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077031 03/18/2014
CITALOPRAM citalopram hydrobromide tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68084-744(NDC:65862-006)
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 K25-31
STARCH, CORN
CROSCARMELLOSE SODIUM
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
HYPROMELLOSE 2910 (6 MPA.S)
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL 400
TITANIUM DIOXIDE
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
Product Characteristics
Color pink (Light Pink) Score 2 pieces
Shape CAPSULE (Biconvex) Size 9mm
Flavor Imprint Code A;0;6
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68084-744-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (68084-744-11)
1 NDC:68084-744-11 1 TABLET, FILM COATED in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (68084-744-01)
Image of Product
(click image for full-size original)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077031 03/17/2014
Labeler — American Health Packaging (929561009)
Establishment
Name Address ID/FEI Operations
American Health Packaging 929561009 repack (68084-737), repack (68084-744)

Revised: 05/2020 American Health Packaging

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