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    Argatroban Monohydrate

    ACTIVE PHARMA INGREDIENTS

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    01 3Ethypharm

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    03 1Medius Ag

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    Ethypharm

    France
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    Virtual BoothEthypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.

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    Regulatory Info : Approved

    Registration Country : Sweden

    Argatroban Monohydrate

    Brand Name : Novastan

    Dosage Form : Infusion Solution

    Dosage Strength : 1mg/ml

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    Approval Date : 19/05/2016

    Application Number : 20141202000017

    Regulatory Info : Approved

    Registration Country : Sweden

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    Ethypharm

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    Regulatory Info : Approved

    Registration Country : Sweden

    Argatroban Monohydrate

    Brand Name : Novastan

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength : 100mg/ml

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    Approval Date : 15/10/2004

    Application Number : 20040607000373

    Regulatory Info : Approved

    Registration Country : Sweden

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    Ethypharm

    France
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    Virtual BoothEthypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.

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    Regulatory Info : Approved

    Registration Country : Sweden

    Argatroban Monohydrate

    Brand Name : Novastan Multidose

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength : 100mg/ml

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    Approval Date : 18/09/2009

    Application Number : 20080315000036

    Regulatory Info : Approved

    Registration Country : Sweden

    Ethypharm

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    Medius Ag

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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Argatrobanum Monohydricum

    Brand Name : Argatra

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength : 100mg/ml

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    Approval Date : 30/12/2014

    Application Number : 62861

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    Cherubino Limited

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    Regulatory Info : Withdrawn

    Registration Country : Malta

    Argatroban

    Brand Name : Exembol Multidose

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength : 100MG/ML

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    Approval Date : 2019-11-01

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    Regulatory Info : Withdrawn

    Registration Country : Malta

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