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    Clopidogrel Hydrochloride

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    REF. STANDARDS & IMPURITIES

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    01 4Krka

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    Krka

    Slovenia
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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 : 2013-09-12

    Application Number : 109556003

    Regulatory Info : Authorized

    Registration Country : Spain

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    Regulatory Info : Authorized

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    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Krka

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

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    Approval Date : 2013-09-12

    Application Number : 109556004

    Regulatory Info : Authorized

    Registration Country : Spain

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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 : 2009-09-21

    Application Number : 9562001

    Regulatory Info : Authorized

    Registration Country : Spain

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    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Krka

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

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    Approval Date : 2024-09-06

    Application Number : 109556007

    Regulatory Info : Authorized

    Registration Country : Spain

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    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Tad

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

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    Approval Date : 2009-09-23

    Application Number : 9555001

    Regulatory Info : Authorized

    Registration Country : Spain

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    Taw Pharma (Ireland) Limited

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    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Taw Pharma

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

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    Approval Date : 2012-10-19

    Application Number : 09559011

    Regulatory Info : Authorized

    Registration Country : Spain

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    Clopidogrel Hydrochloride

    Brand Name : Clopidogrel Taw Pharma

    Dosage Form : Film Coated Tablet

    Dosage Strength : 75MG

    Packaging :

    Approval Date : 2009-09-29

    Application Number : 09559014

    Regulatory Info : Authorized

    Registration Country : Spain

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