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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Maprotiline

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    MARKET PLACE

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    Amdipharm Mercury Company Limited

    United Kingdom
    OTS 2025
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    Amdipharm Mercury Company Limited

    United Kingdom
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Maprotiline Hydrochloride

    Brand Name : Ludiomil

    Dosage Form : Film Coated Tablet

    Dosage Strength : 25mg

    Packaging :

    Approval Date : 23/02/1977

    Application Number : 19770223000016

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Amdipharm Mercury Company Limited

    United Kingdom
    OTS 2025
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    Amdipharm Mercury Company Limited

    United Kingdom
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Maprotiline Hydrochloride

    Brand Name : Ludiomil

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75mg

    Packaging :

    Approval Date : 06/04/1979

    Application Number : 19790406000046

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    03

    Pharmaco Distribution

    South Africa
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    Regulatory Info : Originator

    Registration Country : South Africa

    Maprotiline

    Brand Name : Ludiomil

    Dosage Form : TAB

    Dosage Strength : 25mg

    Packaging : 100X1mg

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    Regulatory Info : Originator

    Registration Country : South Africa

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    Pharmaco Distribution

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    Regulatory Info : Originator

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    Maprotiline

    Brand Name : Ludiomil

    Dosage Form : TAB

    Dosage Strength : 75mg

    Packaging : 30X1mg

    Approval Date :

    Application Number :

    Regulatory Info : Originator

    Registration Country : South Africa

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    Viatris

    U.S.A
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    Viatris

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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Maprotiline Hydrochloride

    Brand Name : Maprotilin Mylan

    Dosage Form : Tablet

    Dosage Strength : 25mg

    Packaging :

    Approval Date : 26/04/1991

    Application Number : 19910426000035

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Viatris

    U.S.A
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    Viatris

    U.S.A
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    • fda
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Maprotiline Hydrochloride

    Brand Name : Maprotilin Mylan

    Dosage Form : Tablet

    Dosage Strength : 75mg

    Packaging :

    Approval Date : 26/04/1991

    Application Number : 19910426000042

    Regulatory Info : Deregistered

    Registration Country : Sweden

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