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    Clopidogrel Hydrochloride

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    REF. STANDARDS & IMPURITIES

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    01 1KRKA, dd Novo mesto

    02 6Krka Dd Novo Mesto

    03 1Sandoz A/S

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    KRKA, dd Novo mesto

    Slovenia
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    KRKA, dd Novo mesto

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    Regulatory Info : Not Marketed

    Registration Country : Norway

    Klopidogrelhydroklorid

    Brand Name : Clopidogrel Krka

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75mg

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    Regulatory Info : Not Marketed

    Registration Country : Norway

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    02

    Krka Dd Novo Mesto

    Slovenia
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    Krka Dd Novo Mesto

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    Regulatory Info : Authorized

    Registration Country : Spain

    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Krka

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

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    Approval Date : 12-09-2013

    Application Number : 109556003

    Regulatory Info : Authorized

    Registration Country : Spain

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    03

    Krka Dd Novo Mesto

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    Regulatory Info : Authorized

    Registration Country : Spain

    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Krka

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

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    Approval Date : 12-09-2013

    Application Number : 109556004

    Regulatory Info : Authorized

    Registration Country : Spain

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    Krka Dd Novo Mesto

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    Regulatory Info : Authorized

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    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Krka D.D.

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

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    Approval Date : 21-09-2009

    Application Number : 9562001

    Regulatory Info : Authorized

    Registration Country : Spain

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    05

    Krka Dd Novo Mesto

    Slovenia
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    Krka Dd Novo Mesto

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    Regulatory Info : Authorized

    Registration Country : Spain

    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Krka

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

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    Approval Date : 06-09-2024

    Application Number : 109556007

    Regulatory Info : Authorized

    Registration Country : Spain

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    06

    Krka Dd Novo Mesto

    Slovenia
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    Krka Dd Novo Mesto

    Slovenia
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    Regulatory Info : Prescription

    Registration Country : Denmark

    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel \"Krka\"

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75mg

    Packaging :

    Approval Date : 23-09-2009

    Application Number : 28104396508

    Regulatory Info : Prescription

    Registration Country : Denmark

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    07

    Krka Dd Novo Mesto

    Slovenia
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    Krka Dd Novo Mesto

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    Regulatory Info : Prescription

    Registration Country : Denmark

    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Krka D.D.

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75mg

    Packaging :

    Approval Date : 21-09-2009

    Application Number : 28104479309

    Regulatory Info : Prescription

    Registration Country : Denmark

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    08

    Sandoz A/S

    Switzerland
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    Regulatory Info : Prescription

    Registration Country : Denmark

    Clopidogrel Hydrochloride

    Brand Name : Cloriocard

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75mg

    Packaging :

    Approval Date : 07-10-2009

    Application Number : 28104375608

    Regulatory Info : Prescription

    Registration Country : Denmark

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    09

    Tad Pharma Gmbh

    Germany
    International Sweetener Colloquium
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    Germany
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    Regulatory Info : Authorized

    Registration Country : Spain

    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Tad

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

    Packaging :

    Approval Date : 23-09-2009

    Application Number : 9555001

    Regulatory Info : Authorized

    Registration Country : Spain

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    10

    Tad Pharma Gmbh

    Germany
    International Sweetener Colloquium
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    Tad Pharma Gmbh

    Germany
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    Regulatory Info : Prescription

    Registration Country : Denmark

    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel \"Tad\"

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75mg

    Packaging :

    Approval Date : 23-09-2009

    Application Number : 28104478809

    Regulatory Info : Prescription

    Registration Country : Denmark

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