NDC 0456-2020

Lexapro

Escitalopram

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

Product ID0456-2020_1174889a-04b7-4b02-a858-5aab5bf2bb13
NDC0456-2020
Product TypeHuman Prescription Drug
Proprietary NameLexapro
Generic NameEscitalopram
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2002-08-14
Marketing CategoryNDA / NDA
Application NumberNDA021323
Labeler NameAllergan, Inc.
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength20 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0456-2020-01

100 TABLET, FILM COATED in 1 BOTTLE (0456-2020-01)
Marketing Start Date2002-08-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0456-2020-63 [00456202063]

Lexapro TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-08-14

NDC 0456-2020-11 [00456202011]

Lexapro TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-12-22

NDC 0456-2020-01 [00456202001]

Lexapro TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021323
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-08-14

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE20 mg/1

OpenFDA Data

SPL SET ID:13bb8267-1cab-43e5-acae-55a4d957630a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250
  • 352272
  • 351249
  • 404420
  • 404408
  • 349332
  • 351285
  • 352273
    • UPC Code
  • 0304562101084

    • Pharmacological Class

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

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

    NDCBrand NameGeneric Name
    0456-2005LexaproESCITALOPRAM
    0456-2010LexaproESCITALOPRAM
    0456-2020LexaproESCITALOPRAM
    33261-699LexaproLexapro
    33261-686LexaproLexapro
    50436-9803LexaproLexapro
    55289-768LexaproLexapro
    55289-828LexaproLexapro
    63629-2981LexaproLexapro
    0093-5850EscitalopramEscitalopram
    0093-5851EscitalopramEscitalopram
    0093-5852EscitalopramEscitalopram
    0143-9807EscitalopramEscitalopram
    0143-9808EscitalopramEscitalopram
    0143-9809EscitalopramEscitalopram
    0615-7720EscitalopramEscitalopram
    0615-7721EscitalopramEscitalopram
    0615-7722EscitalopramEscitalopram
    0615-8348EscitalopramEscitalopram
    0615-8349EscitalopramEscitalopram
    0615-8350EscitalopramEscitalopram
    0615-8365EscitalopramEscitalopram
    0615-8366EscitalopramEscitalopram
    0378-3855Escitalopram Oxalateescitalopram
    0378-3856Escitalopram Oxalateescitalopram
    0378-3857Escitalopram Oxalateescitalopram

    Trademark Results [Lexapro]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    LEXAPRO
    LEXAPRO
    79388487 not registered Live/Pending
    H. Lundbeck A/S
    2023-11-23
    LEXAPRO
    LEXAPRO
    76184942 2684432 Live/Registered
    H. Lundbeck A/S
    2000-12-22
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.