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    Lazertinib

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    LAZERTINIB MESYLATE

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    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 80MG BASE

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    Approval Date : 2024-08-19

    Application Number : 219008

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    LAZERTINIB (LAZERTINIB MESYLATE)

    Brand Name : LAZCLUZE

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    Brand Name : LAZCLUZE

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    Application Number : 2555972

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    Regulatory Info : Authorized

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    Lazertinib

    Brand Name : Lazcluze

    Dosage Form : Film Coated Tablet

    Dosage Strength : 80MG

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    Approval Date : 29-01-2025

    Application Number : 1241886001

    Regulatory Info : Authorized

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    Regulatory Info : Authorized

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    Lazertinib

    Brand Name : Lazcluze

    Dosage Form : Film Coated Tablet

    Dosage Strength : 240MG

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    Approval Date : 29-01-2025

    Application Number : 1241886005

    Regulatory Info : Authorized

    Registration Country : Spain

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    Lazertinib

    Brand Name : Lazcluze

    Dosage Form : Film Coated Tablet

    Dosage Strength : 240mg

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    Approval Date : 20-01-2025

    Application Number : 28107094023

    Regulatory Info : Prescription

    Registration Country : Denmark

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    Regulatory Info : Prescription

    Registration Country : Denmark

    Lazertinib

    Brand Name : Lazcluze

    Dosage Form : Film Coated Tablet

    Dosage Strength : 80mg

    Packaging :

    Approval Date : 20-01-2025

    Application Number : 28107093923

    Regulatory Info : Prescription

    Registration Country : Denmark

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