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    Dacomitinib

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    Pfizer Inc

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    Regulatory Info : RX

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    DACOMITINIB

    Brand Name : VIZIMPRO

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2018-09-27

    Application Number : 211288

    Regulatory Info : RX

    Registration Country : USA

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    DACOMITINIB

    Brand Name : VIZIMPRO

    Dosage Form : TABLET;ORAL

    Dosage Strength : 30MG

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    Approval Date : 2018-09-27

    Application Number : 211288

    Regulatory Info : RX

    Registration Country : USA

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    DACOMITINIB

    Brand Name : VIZIMPRO

    Dosage Form : TABLET;ORAL

    Dosage Strength : 45MG

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    Approval Date : 2018-09-27

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    Regulatory Info : Approved

    Registration Country : Sweden

    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 15mg

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    Approval Date : 02/04/2019

    Application Number : 20180212000013

    Regulatory Info : Approved

    Registration Country : Sweden

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    Regulatory Info : Approved

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    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 30mg

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    Approval Date : 02/04/2019

    Application Number : 20180212000020

    Regulatory Info : Approved

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    Regulatory Info : Approved

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    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 45mg

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    Approval Date : 02/04/2019

    Application Number : 20180212000037

    Regulatory Info : Approved

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    Regulatory Info : Not Marketed

    Registration Country : Norway

    Dacomitinib monohydrate

    Brand Name : Vizimpro

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    Regulatory Info : Not Marketed

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    Regulatory Info : Marketed

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    Brand Name : Vizimpro

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    Dosage Strength : 30mg

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    Approval Date :

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    Regulatory Info : Marketed

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    Regulatory Info : Marketed

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    Dacomitinib monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 45mg

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    Approval Date :

    Application Number :

    Regulatory Info : Marketed

    Registration Country : Norway

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    10

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    Registration Country : Estonia

    Dacomitinib

    Brand Name : Vizimpro

    Dosage Form : Film-Coated Tablet

    Dosage Strength : 15mg

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    Approval Date :

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    Regulatory Info : Prescription

    Registration Country : Estonia

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    Dacomitinib

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    Dosage Form : Film-Coated Tablet

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    Approval Date :

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    Dacomitinib

    Brand Name : Vizimpro

    Dosage Form : Film-Coated Tablet

    Dosage Strength : 45mg

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    Approval Date :

    Application Number :

    Regulatory Info : Prescription

    Registration Country : Estonia

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    13

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    Regulatory Info : Authorized

    Registration Country : Spain

    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 23-05-2019

    Application Number : 1191354002

    Regulatory Info : Authorized

    Registration Country : Spain

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    14

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    Regulatory Info : Authorized

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    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 45MG

    Packaging :

    Approval Date : 23-05-2019

    Application Number : 1191354003

    Regulatory Info : Authorized

    Registration Country : Spain

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    Dacomitinib Monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 15MG

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    Approval Date : 23-05-2019

    Application Number : 1191354001

    Regulatory Info : Authorized

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    Registration Country : Denmark

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    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 15mg

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    Approval Date : 02-04-2019

    Application Number : 28106083818

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    Registration Country : Denmark

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    Brand Name : Vizimpro

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    Dosage Strength : 30mg

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    Approval Date : 02-04-2019

    Application Number : 28106083918

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    Registration Country : Denmark

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    Approval Date : 02-04-2019

    Application Number : 28106084018

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