NDC 71335-0658

Escitalopram

Escitalopram Oxalate

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

Product ID71335-0658_064c64ee-8387-4934-aee9-cc561eb59add
NDC71335-0658
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 NameBryant Ranch Prepack
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength20 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71335-0658-1

60 TABLET, FILM COATED in 1 BOTTLE (71335-0658-1)
Marketing Start Date2018-08-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0658-6 [71335065806]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-01-26

NDC 71335-0658-4 [71335065804]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-01-26

NDC 71335-0658-5 [71335065805]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-01-26

NDC 71335-0658-7 [71335065807]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-01-26

NDC 71335-0658-2 [71335065802]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-01-26

NDC 71335-0658-1 [71335065801]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-01-26

NDC 71335-0658-3 [71335065803]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-01-26

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE20 mg/1

OpenFDA Data

SPL SET ID:69d581c1-9ee5-4d9b-8ee8-fa9d310e8553
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250

    • Pharmacological Class

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

    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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