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    AbbVie Inc

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    Brand Name : LEXAPRO

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    RLD : Yes

    TE Code : AB

    ESCITALOPRAM OXALATE

    AbbVie Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : LEXAPRO

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2002-08-14

    Application Number : 21323

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    02

    Brand Name : LEXAPRO

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Digital Content Digital Content

    RLD : Yes

    TE Code : AB

    ESCITALOPRAM OXALATE

    AbbVie Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : LEXAPRO

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2002-08-14

    Application Number : 21323

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

    Abbvie Company Banner

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    #PipelineProspector

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    03

    Brand Name : LEXAPRO

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag U.S.A
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    Digital Content Digital Content

    RLD : Yes

    TE Code : AB

    ESCITALOPRAM OXALATE

    AbbVie Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : LEXAPRO

    Dosage Strength : EQ 5MG BASE

    Approval Date : 2002-08-14

    Application Number : 21323

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    #PipelineProspector

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