NDC 71335-1002

Escitalopram

Escitalopram

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 ID71335-1002_1d8f7f7a-7891-4d2c-94a7-ae01ecb76a2c
NDC71335-1002
Product TypeHuman Prescription Drug
Proprietary NameEscitalopram
Generic NameEscitalopram
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2013-03-21
Marketing CategoryANDA / ANDA
Application NumberANDA202389
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 Through2023-12-31

Packaging

NDC 71335-1002-1

60 TABLET, FILM COATED in 1 BOTTLE (71335-1002-1)
Marketing Start Date2018-12-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1002-6 [71335100206]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-17

NDC 71335-1002-3 [71335100203]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-17

NDC 71335-1002-2 [71335100202]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-17

NDC 71335-1002-7 [71335100207]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-17

NDC 71335-1002-1 [71335100201]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-17

NDC 71335-1002-5 [71335100205]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-17

NDC 71335-1002-4 [71335100204]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-17

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE20 mg/1

OpenFDA Data

SPL SET ID:d143ec01-9445-42d5-a259-b0b5a7f9445f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250
  • 349332

    • Pharmacological Class

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

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

    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
    0615-8348EscitalopramEscitalopram
    0615-8349EscitalopramEscitalopram
    0615-8350EscitalopramEscitalopram
    0615-8365EscitalopramEscitalopram
    0615-8366EscitalopramEscitalopram
    16729-168EscitalopramEscitalopram
    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
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.