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    Isofosfamide

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    01

    Baxter Medical AB

    U.S.A
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    Regulatory Info : Marketed

    Registration Country : Norway

    Ifosfamide

    Brand Name : Holoxan

    Dosage Form : Injection/Infusion Solution

    Dosage Strength : 1000mg

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    Approval Date :

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    Regulatory Info : Marketed

    Registration Country : Norway

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    02

    Baxter Medical AB

    U.S.A
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    Regulatory Info : Marketed

    Registration Country : Norway

    Ifosfamide

    Brand Name : Holoxan

    Dosage Form : Injection/Infusion Solution

    Dosage Strength : 2000mg

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    Regulatory Info : Marketed

    Registration Country : Norway

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    03

    Baxter Medical AB

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    Regulatory Info : Marketed

    Registration Country : Norway

    Ifosfamide

    Brand Name : Holoxan

    Dosage Form : Injection/Infusion Solution

    Dosage Strength : 500mg

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    Regulatory Info : Marketed

    Registration Country : Norway

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    04

    Baxter A/S

    U.S.A
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    Regulatory Info : Prescription

    Registration Country : Denmark

    Ifosphamide

    Brand Name : Holoxan

    Dosage Form : Injection/Infusion Solution

    Dosage Strength : 1g

    Packaging :

    Approval Date : 28-11-1984

    Application Number : 28101091881

    Regulatory Info : Prescription

    Registration Country : Denmark

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    05

    Baxter A/S

    U.S.A
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    Regulatory Info : Prescription

    Registration Country : Denmark

    Ifosphamide

    Brand Name : Holoxan

    Dosage Form : Injection/Infusion Solution

    Dosage Strength : 2g

    Packaging :

    Approval Date : 28-11-1984

    Application Number : 28101091981

    Regulatory Info : Prescription

    Registration Country : Denmark

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    06

    Baxter A/S

    U.S.A
    International Sweetener Colloquium
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    International Sweetener Colloquium
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    Regulatory Info : Prescription

    Registration Country : Denmark

    Ifosphamide

    Brand Name : Holoxan

    Dosage Form : Injection/Infusion Solution

    Dosage Strength : 500mg

    Packaging :

    Approval Date : 28-11-1984

    Application Number : 28101091781

    Regulatory Info : Prescription

    Registration Country : Denmark

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    07

    Baxter Ag

    Germany
    International Sweetener Colloquium
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    Baxter Ag

    Germany
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    International Sweetener Colloquium
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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Ifosfamide

    Brand Name : Holoxan

    Dosage Form : Powder For Infusion

    Dosage Strength : 500mg

    Packaging :

    Approval Date : 11/09/1979

    Application Number : 41217

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    08

    Baxter Ag

    Germany
    International Sweetener Colloquium
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    International Sweetener Colloquium
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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Ifosfamide

    Brand Name : Holoxan

    Dosage Form : Powder For Infusion

    Dosage Strength : 1g

    Packaging :

    Approval Date : 11/09/1979

    Application Number : 41217

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    09

    Baxter Ag

    Germany
    International Sweetener Colloquium
    Not Confirmed
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    Baxter Ag

    Germany
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    International Sweetener Colloquium
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Ifosfamide

    Brand Name : Holoxan

    Dosage Form : Powder For Infusion

    Dosage Strength : 2g

    Packaging :

    Approval Date : 11/09/1979

    Application Number : 41217

    Regulatory Info : Allowed

    Registration Country : Switzerland

    blank

    Portfolio PDF

    Product Web Link

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    10

    Baxter Holding B.V.

    Germany
    International Sweetener Colloquium
    Not Confirmed
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    Baxter Holding B.V.

    Germany
    arrow
    International Sweetener Colloquium
    Not Confirmed
    • fda
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    Regulatory Info : Authorised

    Registration Country : Malta

    Ifosfamide

    Brand Name : Mitoxana

    Dosage Form : Powder For Concentrate For Injectable Solution And For Infusion

    Dosage Strength : 2G

    Packaging :

    Approval Date : 2007-03-02

    Application Number :

    Regulatory Info : Authorised

    Registration Country : Malta

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