NDC 67046-174

escitalopram oxalate

Escitalopram Oxalate

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

Product ID67046-174_5a05b94a-6dda-572e-e053-2a91aa0a660f
NDC67046-174
Product TypeHuman Prescription Drug
Proprietary Nameescitalopram oxalate
Generic NameEscitalopram Oxalate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-09-25
Marketing CategoryANDA / ANDA
Application NumberANDA090939
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 67046-174-07

7 TABLET in 1 BLISTER PACK (67046-174-07)
Marketing Start Date2017-09-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-174-60 [67046017460]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25

NDC 67046-174-14 [67046017414]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25

NDC 67046-174-15 [67046017415]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25

NDC 67046-174-28 [67046017428]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25

NDC 67046-174-30 [67046017430]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25

NDC 67046-174-07 [67046017407]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25

NDC 67046-174-21 [67046017421]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25

NDC 67046-174-20 [67046017420]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE20 mg/1

OpenFDA Data

SPL SET ID:5a05b94a-6dd9-572e-e053-2a91aa0a660f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250
    • UPC Code
  • 0313668137057

    • Pharmacological Class

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

    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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