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    Atezolizumab

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    01 54F. Hoffmann-La Roche

    02 2Genentech

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    04 1Roche Products (Pty) Ltd

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    01

    F. Hoffmann-La Roche

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    Regulatory Info :

    Registration Country : Norway

    Atezolizumab

    Brand Name : Tecentriq

    Dosage Form : Concentrate for infusion solution, solution

    Dosage Strength : 1,200 mg

    Packaging : Vials 1 20ml

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    Registration Country : Norway

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    Atezolizumab

    Brand Name : Tecentriq

    Dosage Form : Solution for injection

    Dosage Strength : 1,875 mg

    Packaging : Vials 1 15ml

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    Atezolizumab

    Brand Name : Tecentriq

    Dosage Form : Concentrate for infusion solution, solution

    Dosage Strength : 840 mg

    Packaging : Vials 1 14ml

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    Atezolizumabum

    Brand Name : Tecentriq

    Dosage Form : Inf Konz

    Dosage Strength : 1200mg/20ml

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    Regulatory Info : Prescription

    Registration Country : Canada

    ATEZOLIZUMAB

    Brand Name : TECENTRIQ

    Dosage Form : SOLUTION

    Dosage Strength : 840MG/14ML

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    Approval Date :

    Application Number : 2492393

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    06

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    ATEZOLIZUMAB

    Brand Name : TECENTRIQ

    Dosage Form : SOLUTION

    Dosage Strength : 1200MG/20ML

    Packaging : 20ML

    Approval Date :

    Application Number : 2462990

    Regulatory Info : Prescription

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    07

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    ATEZOLIZUMAB

    Brand Name : TECENTRIQ SC

    Dosage Form : SOLUTION

    Dosage Strength : 125MG/ML

    Packaging :

    Approval Date :

    Application Number : 2546310

    Regulatory Info : Prescription

    Registration Country : Canada

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    08

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    Regulatory Info : Originator

    Registration Country : South Africa

    Atezolizumab

    Brand Name : TECENTRIQ 840 MG

    Dosage Form : INF

    Dosage Strength : 840mg

    Packaging : 14X1mg

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    Regulatory Info : Originator

    Registration Country : South Africa

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    09

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    Registration Country : Australia

    atezolizumab

    Brand Name : Tecentriq

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    Dosage Strength :

    Packaging : 1

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Australia

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    10

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    Packaging : 1

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    Application Number :

    Regulatory Info :

    Registration Country : Australia

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    11

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    Regulatory Info :

    Registration Country : Australia

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    12

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    Application Number :

    Regulatory Info :

    Registration Country : Australia

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    13

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    14

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    Application Number : 761034

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    Genentech

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    Regulatory Info :

    Registration Country : USA

    ATEZOLIZUMAB

    Brand Name : TECENTRIQ

    Dosage Form : INJECTABLE; INJECTION

    Dosage Strength : 1200MG/20ML

    Packaging :

    Approval Date :

    Application Number : 761041

    Regulatory Info :

    Registration Country : USA

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    ORIFARM GROUP AS

    Denmark
    Antibody Engineering
    Not Confirmed
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    ORIFARM GROUP AS

    Denmark
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    Antibody Engineering
    Not Confirmed
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    Regulatory Info :

    Registration Country : Norway

    Atezolizumab

    Brand Name : Tecentriq

    Dosage Form : Concentrate for infusion solution, solution

    Dosage Strength : 840 mg

    Packaging : Vials 1 14ml

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Norway

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    ORIFARM GROUP AS

    Denmark
    Antibody Engineering
    Not Confirmed
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    ORIFARM GROUP AS

    Denmark
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    Antibody Engineering
    Not Confirmed
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    Regulatory Info :

    Registration Country : Norway

    Atezolizumab

    Brand Name : Tecentriq

    Dosage Form : Concentrate for infusion solution, solution

    Dosage Strength : 1,200 mg

    Packaging : Vials 1 20ml

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Norway

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    Roche Products (Pty) Ltd

    Country
    Antibody Engineering
    Not Confirmed
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    Roche Products (Pty) Ltd

    Country
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    Antibody Engineering
    Not Confirmed
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    Regulatory Info : Originator

    Registration Country : South Africa

    Atezolizumab

    Brand Name : TECENTRIQ 1 200 MG

    Dosage Form : INF

    Dosage Strength : 1200mg

    Packaging : 20X1mg

    Approval Date :

    Application Number :

    Regulatory Info : Originator

    Registration Country : South Africa

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