NDC 65862-006

Citalopram

Citalopram Hydrobromide

Citalopram is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is Citalopram Hydrobromide.

Product ID65862-006_351ea1bc-a500-4fb6-bb66-5166c82bad80
NDC65862-006
Product TypeHuman Prescription Drug
Proprietary NameCitalopram
Generic NameCitalopram Hydrobromide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2004-10-28
Marketing CategoryANDA / DRUG FOR FURTHER PROCESSING
Application NumberANDA077031
Labeler NameAurobindo Pharma Limited
Substance NameCITALOPRAM HYDROBROMIDE
Active Ingredient Strength20 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 65862-006-01

100 TABLET, FILM COATED in 1 BOTTLE (65862-006-01)
Marketing Start Date2004-10-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65862-006-30 [65862000630]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-10-28

NDC 65862-006-10 [65862000610]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-10-28

NDC 65862-006-53 [65862000653]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-12-09
Marketing End Date2012-08-15

NDC 65862-006-19 [65862000619]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-12-09
Marketing End Date2012-08-15

NDC 65862-006-01 [65862000601]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-10-28

NDC 65862-006-05 [65862000605]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-10-28

NDC 65862-006-90 [65862000690]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-10-28

NDC 65862-006-32 [65862000632]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-10-28

NDC 65862-006-60 [65862000660]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-10-28

Drug Details

Active Ingredients

IngredientStrength
CITALOPRAM HYDROBROMIDE20 mg/1

Medicade Reported Pricing

65862006950 CEFPROZIL 500 MG TABLET

Pricing Unit: EA | Drug Type:

65862006901 CEFPROZIL 500 MG TABLET

Pricing Unit: EA | Drug Type:

65862006801 CEFPROZIL 250 MG TABLET

Pricing Unit: EA | Drug Type:

65862006499 METOPROLOL TARTRATE 100 MG TAB

Pricing Unit: EA | Drug Type:

65862006439 METOPROLOL TARTRATE 100 MG TAB

Pricing Unit: EA | Drug Type:

65862006401 METOPROLOL TARTRATE 100 MG TAB

Pricing Unit: EA | Drug Type:

65862006399 METOPROLOL TARTRATE 50 MG TAB

Pricing Unit: EA | Drug Type:

65862006359 METOPROLOL TARTRATE 50 MG TAB

Pricing Unit: EA | Drug Type:

65862006301 METOPROLOL TARTRATE 50 MG TAB

Pricing Unit: EA | Drug Type:

65862006299 METOPROLOL TARTRATE 25 MG TAB

Pricing Unit: EA | Drug Type:

65862006201 METOPROLOL TARTRATE 25 MG TAB

Pricing Unit: EA | Drug Type:

65862006130 FLUCONAZOLE 200 MG TABLET

Pricing Unit: EA | Drug Type:

65862006011 FLUCONAZOLE 150 MG TABLET

Pricing Unit: EA | Drug Type:

65862000605 CITALOPRAM HBR 20 MG TABLET

Pricing Unit: EA | Drug Type:

65862000601 CITALOPRAM HBR 20 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Citalopram" or generic name "Citalopram Hydrobromide"

NDCBrand NameGeneric Name
0054-0062CitalopramCitalopram
0121-0848CitalopramCitalopram Hydrobromide
0121-1696CitalopramCitalopram Hydrobromide
0185-0371CitalopramCitalopram Hydrobromide
0185-0372CitalopramCitalopram Hydrobromide
0185-0373CitalopramCitalopram Hydrobromide
0378-6231Citalopramcitalopram
0378-6232Citalopramcitalopram
0378-6233Citalopramcitalopram
0615-6510CitalopramCitalopram
0615-6511CitalopramCitalopram
0615-6512CitalopramCitalopram
0615-8022CitalopramCitalopram Hydrobromide
0615-8023CitalopramCitalopram Hydrobromide
0615-8141CitalopramCitalopram Hydrobromide
0713-4740CitalopramCitalopram Tablets
68071-1970CitalopramCitalopram
68071-3042CitalopramCitalopram
68071-3034CitalopramCitalopram
68071-3357CitalopramCitalopram
68071-4291CitalopramCitalopram
68071-4604CitalopramCitalopram
68071-4477CitalopramCitalopram
68071-4324CitalopramCitalopram
68084-737CitalopramCitalopram
68084-744CitalopramCitalopram
68788-6810CitalopramCitalopram
68788-0005CitalopramCitalopram
68788-0007CitalopramCitalopram
69097-822CitalopramCitalopram
69097-824CitalopramCitalopram
69097-823CitalopramCitalopram
70518-0449CitalopramCitalopram
70518-0561CitalopramCitalopram
71335-0541CitalopramCitalopram
71335-0573CitalopramCitalopram
71335-0712CitalopramCitalopram
71335-0656CitalopramCitalopram
0713-4741CitalopramCitalopram
0713-4742CitalopramCitalopram
10544-149CitalopramCitalopram
10544-179CitalopramCitalopram
10544-006CitalopramCitalopram
10544-150CitalopramCitalopram
10544-182CitalopramCitalopram
13107-005CitalopramCitalopram
13107-007CitalopramCitalopram
13107-006CitalopramCitalopram
21695-031CitalopramCitalopram
21695-032CitalopramCitalopram
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