NDC 13668-135

escitalopram oxalate

Escitalopram Oxalate

escitalopram oxalate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Torrent Pharmaceuticals Limited. The primary component is Escitalopram Oxalate.

Product ID13668-135_4e26de4d-6afd-4037-a52a-2d7778aaf92f
NDC13668-135
Product TypeHuman Prescription Drug
Proprietary Nameescitalopram oxalate
Generic NameEscitalopram Oxalate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2012-09-11
Marketing CategoryANDA / ANDA
Application NumberANDA090939
Labeler NameTorrent Pharmaceuticals Limited
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength5 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 13668-135-01

100 TABLET in 1 BOTTLE (13668-135-01)
Marketing Start Date2012-09-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 13668-135-01 [13668013501]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11

NDC 13668-135-05 [13668013505]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11

NDC 13668-135-10 [13668013510]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11

NDC 13668-135-30 [13668013530]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-11

NDC 13668-135-40 [13668013540]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-11

NDC 13668-135-74 [13668013574]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-11

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE5 mg/1

OpenFDA Data

SPL SET ID:068bb338-23f3-4278-958b-c34b40456024
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250
  • 349332
  • 351249
    • UPC Code
  • 0313668136050
  • 0313668135053
  • 0313668137057

    • Pharmacological Class

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

    Medicade Reported Pricing

    13668013510 ESCITALOPRAM 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    13668013505 ESCITALOPRAM 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    13668013501 ESCITALOPRAM 5 MG TABLET

    Pricing Unit: EA | Drug Type:

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

    NDCBrand NameGeneric Name
    0121-0852Escitalopram OxalateEscitalopram Oxalate
    0378-3855Escitalopram Oxalateescitalopram
    0378-3856Escitalopram Oxalateescitalopram
    0378-3857Escitalopram Oxalateescitalopram
    0904-6426escitalopram oxalateescitalopram oxalate
    0904-6427escitalopram oxalateescitalopram oxalate
    10544-224escitalopram oxalateescitalopram oxalate
    10544-225escitalopram oxalateescitalopram oxalate
    10544-230escitalopram oxalateescitalopram oxalate
    10544-968Escitalopram Oxalateescitalopram
    10544-969Escitalopram Oxalateescitalopram
    13668-135escitalopram oxalateescitalopram oxalate
    13668-136escitalopram oxalateescitalopram oxalate
    13668-137escitalopram oxalateescitalopram oxalate
    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
    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
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