NDC 67046-173

Escitalopram Oxalate

Escitalopram

Escitalopram Oxalate is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Escitalopram Oxalate.

Product ID67046-173_5a058aa9-323a-4ce6-e053-2991aa0a90ea
NDC67046-173
Product TypeHuman Prescription Drug
Proprietary NameEscitalopram Oxalate
Generic NameEscitalopram
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-09-25
Marketing CategoryNDA / NDA
Application NumberNDA021323
Labeler NameContract Pharmacy Services-PA
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength20 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 67046-173-30

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-173-30)
Marketing Start Date2017-09-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-173-28 [67046017328]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Marketing End Date2020-01-31

NDC 67046-173-07 [67046017307]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Marketing End Date2020-01-31

NDC 67046-173-60 [67046017360]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Marketing End Date2020-01-31

NDC 67046-173-20 [67046017320]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Marketing End Date2020-01-31

NDC 67046-173-30 [67046017330]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Marketing End Date2020-01-31

NDC 67046-173-14 [67046017314]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Marketing End Date2020-01-31

NDC 67046-173-15 [67046017315]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Marketing End Date2020-01-31

NDC 67046-173-21 [67046017321]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Marketing End Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE20 mg/1

OpenFDA Data

SPL SET ID:5a058aa9-3239-4ce6-e053-2991aa0a90ea
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250
    • UPC Code
  • 0303783857107

    • Pharmacological Class

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

    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
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