NDC 65162-019

Escitalopram Oxalate

Escitalopram Oxalate

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

Product ID65162-019_5d472ade-4b24-4f73-bb8e-cbea46209ca7
NDC65162-019
Product TypeHuman Prescription Drug
Proprietary NameEscitalopram Oxalate
Generic NameEscitalopram Oxalate
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-05-17
Marketing CategoryANDA / ANDA
Application NumberANDA205619
Labeler NameAmneal Pharmaceuticals LLC
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength5 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 65162-019-03

30 TABLET, FILM COATED in 1 BOTTLE (65162-019-03)
Marketing Start Date2017-05-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65162-019-09 [65162001909]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA205619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-05-17

NDC 65162-019-03 [65162001903]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA205619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-05-17

NDC 65162-019-11 [65162001911]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA205619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-05-17

NDC 65162-019-50 [65162001950]

Escitalopram Oxalate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA205619
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-05-17

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE5 mg/1

OpenFDA Data

SPL SET ID:8704d062-fa91-4224-9dec-41664d20ee6b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250
  • 349332
  • 351249
  • UPC Code
  • 0365162020038
  • 0365162021035
  • 0365162019032
  • Pharmacological Class

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

    Medicade Reported Pricing

    65162019050 NAPROXEN 500 MG TABLET

    Pricing Unit: EA | Drug Type:

    65162019011 NAPROXEN 500 MG TABLET

    Pricing Unit: EA | Drug Type:

    65162019010 NAPROXEN 500 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

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