NDC 65862-373

Escitalopram

Escitalopram Oxalate

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

Product ID65862-373_01edb108-693a-47f1-ae29-9e2a75f1b274
NDC65862-373
Product TypeHuman Prescription Drug
Proprietary NameEscitalopram
Generic NameEscitalopram Oxalate
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2012-09-11
Marketing CategoryANDA / ANDA
Application NumberANDA090432
Labeler NameAurobindo Pharma Limited
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 65862-373-01

100 TABLET, FILM COATED in 1 BOTTLE (65862-373-01)
Marketing Start Date2012-09-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65862-373-01 [65862037301]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11

NDC 65862-373-10 [65862037310]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-11

NDC 65862-373-90 [65862037390]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-11

NDC 65862-373-05 [65862037305]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11

NDC 65862-373-30 [65862037330]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-11

NDC 65862-373-19 [65862037319]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-11

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE5 mg/1

OpenFDA Data

SPL SET ID:d5fbc8ce-bd41-4bd0-b413-0dea97e596c3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250
  • 349332
  • 351249
  • UPC Code
  • 0365862373014
  • Pharmacological Class

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

    Medicade Reported Pricing

    65862037305 ESCITALOPRAM 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    65862037301 ESCITALOPRAM 5 MG TABLET

    Pricing Unit: EA | Drug Type:

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

    NDCBrand NameGeneric Name
    0093-5850EscitalopramEscitalopram
    0093-5851EscitalopramEscitalopram
    0093-5852EscitalopramEscitalopram
    0143-9807EscitalopramEscitalopram
    0143-9808EscitalopramEscitalopram
    0143-9809EscitalopramEscitalopram
    0615-7720EscitalopramEscitalopram
    0615-7721EscitalopramEscitalopram
    0615-7722EscitalopramEscitalopram
    0615-7953EscitalopramEscitslopram
    0615-7954EscitalopramEscitslopram
    0615-7955EscitalopramEscitslopram
    68001-195EscitalopramEscitalopram
    68001-196EscitalopramEscitalopram
    68001-197EscitalopramEscitalopram
    68071-2051EscitalopramEscitalopram
    68071-3069EscitalopramEscitalopram
    68071-2035EscitalopramEscitalopram
    68071-4332EscitalopramEscitalopram
    68071-4484EscitalopramEscitalopram
    68084-617EscitalopramEscitalopram
    68084-618EscitalopramEscitalopram
    68180-135EscitalopramEscitalopram
    68180-136EscitalopramEscitalopram
    68180-137EscitalopramEscitalopram
    68258-7128EscitalopramEscitalopram
    68382-103escitalopramescitalopram
    68382-104escitalopramescitalopram
    68382-102escitalopramescitalopram
    68788-6837EscitalopramEscitalopram
    68788-6403EscitalopramEscitalopram
    68788-6783EscitalopramEscitalopram
    68788-9302EscitalopramEscitalopram
    68788-9456EscitalopramEscitalopram
    68788-9714EscitalopramEscitalopram
    70518-0692EscitalopramEscitalopram
    70518-1110EscitalopramEscitalopram
    70518-0758EscitalopramEscitalopram
    70518-1103EscitalopramEscitalopram
    70518-1857EscitalopramEscitalopram
    70518-1876EscitalopramEscitalopram
    70518-1785EscitalopramEscitalopram
    70518-1805EscitalopramEscitalopram
    70771-1145escitalopramescitalopram
    70771-1146escitalopramescitalopram
    70771-1147escitalopramescitalopram
    70934-112EscitalopramEscitalopram
    71205-168EscitalopramEscitalopram
    71205-193EscitalopramEscitalopram
    71335-0658EscitalopramEscitalopram

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