NDC 68788-6810

Citalopram

Citalopram

Citalopram is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Citalopram Hydrobromide.

Product ID68788-6810_ca87bc78-17c8-4b52-867a-ca3f71277acd
NDC68788-6810
Product TypeHuman Prescription Drug
Proprietary NameCitalopram
Generic NameCitalopram
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-11-07
Marketing CategoryANDA / ANDA
Application NumberANDA077289
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameCITALOPRAM HYDROBROMIDE
Active Ingredient Strength10 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-6810-6

60 TABLET in 1 BOTTLE (68788-6810-6)
Marketing Start Date2016-11-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-6810-1 [68788681001]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077289
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-07
Marketing End Date2019-07-30

NDC 68788-6810-6 [68788681006]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077289
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-07
Marketing End Date2019-07-30

NDC 68788-6810-8 [68788681008]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077289
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-07
Marketing End Date2019-07-30

NDC 68788-6810-3 [68788681003]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077289
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-07
Marketing End Date2019-07-30

NDC 68788-6810-9 [68788681009]

Citalopram TABLET
Marketing CategoryANDA
Application NumberANDA077289
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-07
Marketing End Date2019-07-30

Drug Details

Active Ingredients

IngredientStrength
CITALOPRAM HYDROBROMIDE10 mg/1

OpenFDA Data

SPL SET ID:702c58a6-24a8-4ece-8d10-46950b01cad0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 283672
  • Pharmacological Class

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

    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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.