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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Azilsartan Medoxomil Potassium

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    Hasten Biopharmaceutic (Switzerland) Ag

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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Azilsartan Medoxomil

    Brand Name : Hanarbe

    Dosage Form : Tablet

    Dosage Strength : 20mg

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    Approval Date : 08/08/2024

    Application Number : 69936

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    Azilsartan Medoxomil

    Brand Name : Hanarbe

    Dosage Form : Tablet

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    Approval Date : 08/08/2024

    Application Number : 69936

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    Registration Country : Switzerland

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    Azilsartan Medoxomil

    Brand Name : Hanarbe

    Dosage Form : Tablet

    Dosage Strength : 80mg

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    Approval Date : 08/08/2024

    Application Number : 69936

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    Registration Country : Switzerland

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    Registration Country : Estonia

    Azilsartan medoxomil

    Brand Name : Edarbi

    Dosage Form : Tablet

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    Regulatory Info : Prescription

    Registration Country : Estonia

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    Brand Name : Edarbi

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    Registration Country : Estonia

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    Azilsartan medoxomil

    Brand Name : Edarbi

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    Regulatory Info : Authorized

    Registration Country : Spain

    Azilsartan Medoxomil

    Brand Name : Edarbi

    Dosage Form : Tablet

    Dosage Strength : 40MG

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    Approval Date : 06-03-2012

    Application Number : 11734006

    Regulatory Info : Authorized

    Registration Country : Spain

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    Brand Name : Edarbi

    Dosage Form : Tablet

    Dosage Strength : 20MG

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    Approval Date : 06-03-2012

    Application Number : 11734002

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    Registration Country : Spain

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    Azilsartan Medoxomil

    Brand Name : Edarbi

    Dosage Form : Tablet

    Dosage Strength : 80MG

    Packaging :

    Approval Date : 06-03-2012

    Application Number : 11734009

    Regulatory Info : Authorized

    Registration Country : Spain

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    Registration Country : Denmark

    Azilsartan Kamedoxomil

    Brand Name : Edarbi

    Dosage Form : Tablet

    Dosage Strength : 20mg

    Packaging :

    Approval Date : 09-12-2011

    Application Number : 28104781110

    Regulatory Info : Prescription

    Registration Country : Denmark

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