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    Dacomitinib

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    01

    Pfizer Europe MA EEIG

    U.S.A
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    Pfizer Europe MA EEIG

    U.S.A
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    Regulatory Info : Not Marketed

    Registration Country : Norway

    Dacomitinib monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 15mg

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    Approval Date :

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    Regulatory Info : Not Marketed

    Registration Country : Norway

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    02

    Pfizer Europe MA EEIG

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    Pfizer Europe MA EEIG

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    Regulatory Info : Marketed

    Registration Country : Norway

    Dacomitinib monohydrate

    Brand Name : Vizimpro

    Dosage Form : Film Coated Tablet

    Dosage Strength : 30mg

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    Approval Date :

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    Regulatory Info : Marketed

    Registration Country : Norway

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    03

    Pfizer Europe MA EEIG

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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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    Regulatory Info : Marketed

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    04

    Pfizer Europe Ma Eeig

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    Regulatory Info : Prescription

    Registration Country : Estonia

    Dacomitinib

    Brand Name : Vizimpro

    Dosage Form : Film-Coated Tablet

    Dosage Strength : 15mg

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    Approval Date :

    Application Number :

    Regulatory Info : Prescription

    Registration Country : Estonia

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    05

    Pfizer Europe Ma Eeig

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    Regulatory Info : Prescription

    Registration Country : Estonia

    Dacomitinib

    Brand Name : Vizimpro

    Dosage Form : Film-Coated Tablet

    Dosage Strength : 30mg

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info : Prescription

    Registration Country : Estonia

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    06

    Pfizer Europe Ma Eeig

    U.S.A
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    Pfizer Europe Ma Eeig

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    Regulatory Info : Prescription

    Registration Country : Estonia

    Dacomitinib

    Brand Name : Vizimpro

    Dosage Form : Film-Coated Tablet

    Dosage Strength : 45mg

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info : Prescription

    Registration Country : Estonia

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    07

    Pfizer Europe Ma Eeig

    U.S.A
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    Pfizer Europe Ma Eeig

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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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    08

    Pfizer Europe Ma Eeig

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    ASPEN
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    Pfizer Europe Ma Eeig

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    ASPEN
    Not Confirmed
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    Regulatory Info : Authorized

    Registration Country : Spain

    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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    09

    Pfizer Europe Ma Eeig

    U.S.A
    ASPEN
    Not Confirmed
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    Pfizer Europe Ma Eeig

    U.S.A
    arrow
    ASPEN
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : Authorized

    Registration Country : Spain

    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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    10

    Pfizer Europe Ma Eeig

    U.S.A
    ASPEN
    Not Confirmed
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    Pfizer Europe Ma Eeig

    U.S.A
    arrow
    ASPEN
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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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