NDC 13107-007

Citalopram

Citalopram

Citalopram is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Aurolife Pharma Llc. The primary component is Citalopram Hydrobromide.

Product ID13107-007_2627f188-05c8-44ac-845e-80678a0c2fdd
NDC13107-007
Product TypeHuman Prescription Drug
Proprietary NameCitalopram
Generic NameCitalopram
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-01-01
Marketing CategoryANDA / ANDA
Application NumberANDA077031
Labeler NameAurolife Pharma LLC
Substance NameCITALOPRAM HYDROBROMIDE
Active Ingredient Strength40 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 13107-007-90

90 TABLET in 1 BOTTLE (13107-007-90)
Marketing Start Date2009-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 13107-007-10 [13107000710]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-01-01
Inactivation Date2020-01-31

NDC 13107-007-90 [13107000790]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-01-01
Inactivation Date2020-01-31

NDC 13107-007-32 [13107000732]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-01-01
Inactivation Date2020-01-31

NDC 13107-007-01 [13107000701]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-01-01
Inactivation Date2020-01-31

NDC 13107-007-60 [13107000760]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-01-01
Inactivation Date2020-01-31

NDC 13107-007-05 [13107000705]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-01-01
Inactivation Date2020-01-31

NDC 13107-007-30 [13107000730]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CITALOPRAM HYDROBROMIDE40 mg/1

OpenFDA Data

SPL SET ID:9f5a14c2-b460-402e-acb4-04402278e64b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 309314
  • 283672
  • 200371
    • UPC Code
  • 0313107006012
  • 0313107005015
  • 0313107007019

    • Pharmacological Class

    • Serotonin Reuptake Inhibitor [EPC]
    • Serotonin Uptake Inhibitors [MoA]

    Medicade Reported Pricing

    13107007701 CIPROFLOXACIN HCL 500 MG TAB

    Pricing Unit: EA | Drug Type:

    13107007501 BUTALBITAL-ACETAMINOPHEN-CAFFEINE 50-325-40 MG CAPSULE

    Pricing Unit: EA | Drug Type:

    13107007401 DEXTROAMP-AMPHETAMIN 30 MG TAB

    Pricing Unit: EA | Drug Type:

    13107007301 DEXTROAMP-AMPHETAMIN 20 MG TAB

    Pricing Unit: EA | Drug Type:

    13107007201 DEXTROAMP-AMPHETAMIN 15 MG TAB

    Pricing Unit: EA | Drug Type:

    13107007001 DEXTROAMP-AMPHETAMIN 10 MG TAB

    Pricing Unit: EA | Drug Type:

    13107000705 CITALOPRAM HBR 40 MG TABLET

    Pricing Unit: EA | Drug Type:

    13107000701 CITALOPRAM HBR 40 MG TABLET

    Pricing Unit: EA | Drug Type:

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

    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
    0713-4741CitalopramCitalopram Tablet
    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
    0713-4742CitalopramCitalopram
    10544-149CitalopramCitalopram
    10544-179CitalopramCitalopram
    10544-006CitalopramCitalopram
    10544-150CitalopramCitalopram
    10544-182CitalopramCitalopram
    13107-005CitalopramCitalopram
    13107-007CitalopramCitalopram
    13107-006CitalopramCitalopram
    21695-031CitalopramCitalopram
    21695-032CitalopramCitalopram
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