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    Inotuzumab ozogamicin

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    Pfizer Consumer Healthcare

    Canada
    The Generic Rx Session
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    The Generic Rx Session
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    Regulatory Info :

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    inotuzumab ozogamicin

    Brand Name : Besponsa

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    Registration Country : Australia

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    Pfizer Consumer Healthcare

    Canada
    The Generic Rx Session
    Not Confirmed
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    Pfizer Consumer Healthcare

    Canada
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    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info :

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    inotuzumab ozogamicin

    Brand Name : Besponsa

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    Packaging : 1

    Approval Date :

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    Regulatory Info :

    Registration Country : Australia

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    03

    Pfizer Consumer Healthcare

    Canada
    The Generic Rx Session
    Not Confirmed
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    Pfizer Consumer Healthcare

    Canada
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    inotuzumab ozogamicin

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    Packaging : 1

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    Regulatory Info :

    Registration Country : Australia

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    04

    Pfizer Consumer Healthcare

    Canada
    The Generic Rx Session
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    Pfizer Consumer Healthcare

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    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
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    inotuzumab ozogamicin

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    Packaging : 1

    Approval Date :

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    Regulatory Info :

    Registration Country : Australia

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    Pfizer Inc

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    Inotuzumabum ozogamicinum

    Brand Name : Besponsa

    Dosage Form : Dry Sub

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    06

    Pfizer Inc

    U.S.A
    The Generic Rx Session
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    Pfizer Inc

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    The Generic Rx Session
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    INOTUZUMAB OZOGAMICIN

    Brand Name : BESPONSA

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 0.9MG/VIAL

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    Approval Date :

    Application Number : 2473909

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    Registration Country : Canada

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    07

    Wyeth Pharmaceuticals Inc

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Registration Country : USA

    INOTUZUMAB OZOGAMICIN

    Brand Name : BESPONSA

    Dosage Form : POWDER, FOR INJECTION SOLUTION, LYOPHILIZED POWDER

    Dosage Strength : 0.9/MG/VIAL

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    Approval Date :

    Application Number : 761040

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    Registration Country : USA

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