Citalopram (Page 10 of 10)

PACKAGE/LABEL DISPLAY PANEL – Carton – 10 mg

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

Citalopram Tablet, USP

10 mg

PACKAGE/LABEL DISPLAY PANEL – Carton – 20 mg

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

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)

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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)

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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