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    Dacomitinib

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    Pfizer Europe MA EEIG

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    Regulatory Info : Not Marketed

    Registration Country : Norway

    Dacomitinib monohydrate

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    Dosage Form : Film Coated Tablet

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    Regulatory Info : Marketed

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    Dacomitinib

    Brand Name : Vizimpro

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    Regulatory Info : Authorized

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    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 30MG

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    Approval Date : 23-05-2019

    Application Number : 1191354002

    Regulatory Info : Authorized

    Registration Country : Spain

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    Regulatory Info : Authorized

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    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 45MG

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    Approval Date : 23-05-2019

    Application Number : 1191354003

    Regulatory Info : Authorized

    Registration Country : Spain

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    Pfizer Europe Ma Eeig

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    BioProcess International US West
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    BioProcess International US West
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    Regulatory Info : Authorized

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    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 23-05-2019

    Application Number : 1191354001

    Regulatory Info : Authorized

    Registration Country : Spain

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    Pfizer Europe Ma Eeig

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    Regulatory Info : Prescription

    Registration Country : Denmark

    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 15mg

    Packaging :

    Approval Date : 02-04-2019

    Application Number : 28106083818

    Regulatory Info : Prescription

    Registration Country : Denmark

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