NDC 76282-249

Escitalopram oxalate

Escitalopram

Escitalopram oxalate is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Exelan Pharmaceuticals Inc.. The primary component is Escitalopram Oxalate.

Product ID76282-249_2941fd5e-feb8-4c2a-a0f8-7e14d61ad7af
NDC76282-249
Product TypeHuman Prescription Drug
Proprietary NameEscitalopram oxalate
Generic NameEscitalopram
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2012-10-01
Marketing CategoryANDA / ANDA
Application NumberANDA078604
Labeler NameExelan Pharmaceuticals Inc.
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength5 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 76282-249-01

100 TABLET, FILM COATED in 1 BOTTLE (76282-249-01)
Marketing Start Date2012-10-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 76282-249-30 [76282024930]

Escitalopram oxalate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-10-01

NDC 76282-249-90 [76282024990]

Escitalopram oxalate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-10-01

NDC 76282-249-10 [76282024910]

Escitalopram oxalate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-10-01

NDC 76282-249-01 [76282024901]

Escitalopram oxalate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-10-01

NDC 76282-249-05 [76282024905]

Escitalopram oxalate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-10-01

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE5 mg/1

OpenFDA Data

SPL SET ID:8a3f4bc9-cd6e-49b1-ab6c-982b70f51fd2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250
  • 349332
  • 351249
  • UPC Code
  • 0376282250908
  • 0376282251905
  • 0376282249902
  • Pharmacological Class

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

    Medicade Reported Pricing

    76282024990 ESCITALOPRAM 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    76282024930 ESCITALOPRAM 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    76282024910 ESCITALOPRAM 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Escitalopram oxalate" or generic name "Escitalopram"

    NDCBrand NameGeneric Name
    0121-0852Escitalopram OxalateEscitalopram Oxalate
    0378-3855Escitalopram Oxalateescitalopram
    0378-3856Escitalopram Oxalateescitalopram
    0378-3857Escitalopram Oxalateescitalopram
    68071-3283Escitalopram OxalateEscitalopram Oxalate
    68071-3312escitalopram oxalateescitalopram oxalate
    68071-3265escitalopram oxalateescitalopram oxalate
    68071-4210escitalopram oxalateescitalopram oxalate
    68645-519Escitalopram OxalateEscitalopram Oxalate
    68645-520Escitalopram OxalateEscitalopram Oxalate
    68788-6978escitalopram oxalateescitalopram oxalate
    69097-848Escitalopram OxalateEscitalopram Oxalate
    69097-849Escitalopram OxalateEscitalopram Oxalate
    69097-847Escitalopram OxalateEscitalopram Oxalate
    70518-0467escitalopram oxalateescitalopram oxalate
    70518-0472escitalopram oxalateescitalopram oxalate
    70518-0439escitalopram oxalateescitalopram oxalate
    70518-1315escitalopram oxalateescitalopram oxalate
    70518-0972Escitalopram OxalateEscitalopram Oxalate
    70518-0791escitalopram oxalateescitalopram oxalate
    70518-1291escitalopram oxalateescitalopram oxalate
    70518-1697escitalopram oxalateescitalopram oxalate
    70934-060escitalopram oxalateescitalopram oxalate
    70934-089escitalopram oxalateescitalopram oxalate
    70934-163escitalopram oxalateescitalopram oxalate
    71335-0685escitalopram oxalateescitalopram oxalate
    76282-251Escitalopram oxalateEscitalopram oxalate
    76282-249Escitalopram oxalateEscitalopram oxalate
    76282-250Escitalopram oxalateEscitalopram oxalate
    0904-6426escitalopram oxalateescitalopram oxalate
    0904-6427escitalopram oxalateescitalopram oxalate
    10544-968Escitalopram OxalateEscitalopram Oxalate
    10544-224escitalopram oxalateescitalopram oxalate
    10544-230escitalopram oxalateescitalopram oxalate
    10544-969Escitalopram OxalateEscitalopram Oxalate
    10544-225escitalopram oxalateescitalopram oxalate
    13668-135escitalopram oxalateescitalopram oxalate
    13668-137escitalopram oxalateescitalopram oxalate
    13668-136escitalopram oxalateescitalopram oxalate
    31722-569Escitalopram OxalateEscitalopram Oxalate
    33261-955escitalopram oxalateescitalopram oxalate
    33342-036Escitalopram OxalateEscitalopram Oxalate
    33342-038Escitalopram OxalateEscitalopram Oxalate
    33342-037Escitalopram OxalateEscitalopram Oxalate
    43063-761escitalopram oxalateescitalopram oxalate
    50090-2752escitalopram oxalateescitalopram oxalate
    51079-544Escitalopram OxalateEscitalopram Oxalate
    51079-543Escitalopram OxalateEscitalopram Oxalate
    55154-5386Escitalopram OxalateEscitalopram Oxalate
    54838-551Escitalopram OxalateEscitalopram Oxalate

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