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    Rofecoxib

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    Mepro Pharmaceuticals

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    Regulatory Info : DISCN

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    ROFECOXIB

    Brand Name : VIOXX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG

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    Approval Date : 1999-05-20

    Application Number : 21042

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    06

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    Regulatory Info : DISCN

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    ROFECOXIB

    Brand Name : VIOXX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG

    Packaging :

    Approval Date : 1999-05-20

    Application Number : 21042

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Merck & Co

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    Merck & Co

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    ROFECOXIB

    Brand Name : VIOXX

    Dosage Form : TABLET;ORAL

    Dosage Strength : 50MG

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    Approval Date : 2000-02-25

    Application Number : 21042

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Merck & Co

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    Regulatory Info : DISCN

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    ROFECOXIB

    Brand Name : VIOXX

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 12.5MG/5ML

    Packaging :

    Approval Date : 1999-05-20

    Application Number : 21052

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Merck & Co

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    Merck & Co

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    The MedTech Conference
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    Regulatory Info : DISCN

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    ROFECOXIB

    Brand Name : VIOXX

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 25MG/5ML

    Packaging :

    Approval Date : 1999-05-20

    Application Number : 21052

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Merck & Co

    U.S.A
    The MedTech Conference
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    Merck & Co

    U.S.A
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    The MedTech Conference
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    Regulatory Info :

    Registration Country : USA

    ROFECOXIB

    Brand Name : VIOXX

    Dosage Form : TABLET; ORAL

    Dosage Strength : 12.5MG

    Packaging :

    Approval Date :

    Application Number : 21647

    Regulatory Info :

    Registration Country : USA

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    11

    Merck & Co

    U.S.A
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    Merck & Co

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    The MedTech Conference
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    ROFECOXIB

    Brand Name : VIOXX

    Dosage Form : TABLET; ORAL

    Dosage Strength : 25MG

    Packaging :

    Approval Date :

    Application Number : 21647

    Regulatory Info :

    Registration Country : USA

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    12

    Merck & Co

    U.S.A
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    Merck & Co

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    The MedTech Conference
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    Regulatory Info :

    Registration Country : USA

    ROFECOXIB

    Brand Name : VIOXX

    Dosage Form : TABLET; ORAL

    Dosage Strength : 50MG

    Packaging :

    Approval Date :

    Application Number : 21647

    Regulatory Info :

    Registration Country : USA

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    13

    Merck & Co

    U.S.A
    The MedTech Conference
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    Merck & Co

    U.S.A
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    The MedTech Conference
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Rofecoxib

    Brand Name : Ceoxx

    Dosage Form : Tablet

    Dosage Strength : 25mg

    Packaging :

    Approval Date : 25/01/2002

    Application Number : 20020125000208

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    14

    Merck & Co

    U.S.A
    The MedTech Conference
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    Merck & Co

    U.S.A
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    The MedTech Conference
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Rofecoxib

    Brand Name : Ceoxx

    Dosage Form : Tablet

    Dosage Strength : 50mg

    Packaging :

    Approval Date : 25/01/2002

    Application Number : 20020125000215

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    15

    Merck & Co

    U.S.A
    The MedTech Conference
    Not Confirmed
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    Merck & Co

    U.S.A
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    The MedTech Conference
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Rofecoxib

    Brand Name : Vioxx

    Dosage Form : Tablet

    Dosage Strength : 12.5mg

    Packaging :

    Approval Date : 22/10/1999

    Application Number : 19991022000247

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    16

    Merck & Co

    U.S.A
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Rofecoxib

    Brand Name : Vioxx

    Dosage Form : Oral Suspension

    Dosage Strength : 2.5mg/ml

    Packaging :

    Approval Date : 22/10/1999

    Application Number : 19991022000261

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    17

    Merck & Co

    U.S.A
    The MedTech Conference
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    Merck & Co

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    The MedTech Conference
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Rofecoxib

    Brand Name : Vioxx

    Dosage Form : Tablet

    Dosage Strength : 25mg

    Packaging :

    Approval Date : 22/10/1999

    Application Number : 19991022000254

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    18

    ORIFARM GROUP AS

    Denmark
    The MedTech Conference
    Not Confirmed
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    ORIFARM GROUP AS

    Denmark
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    The MedTech Conference
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Rofecoxib

    Brand Name : Vioxx

    Dosage Form : Tablet

    Dosage Strength : 12.5mg

    Packaging :

    Approval Date : 01/11/2002

    Application Number : 20021101000304

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    19

    ORIFARM GROUP AS

    Denmark
    The MedTech Conference
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    ORIFARM GROUP AS

    Denmark
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    The MedTech Conference
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Rofecoxib

    Brand Name : Vioxx

    Dosage Form : Tablet

    Dosage Strength : 12.5mg

    Packaging :

    Approval Date : 21/01/2004

    Application Number : 20040121000071

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    20

    Pharmachim Ab

    Country
    The MedTech Conference
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    Pharmachim Ab

    Country
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    The MedTech Conference
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Rofecoxib

    Brand Name : Vioxx

    Dosage Form : Tablet

    Dosage Strength : 12.5mg

    Packaging :

    Approval Date : 20/02/2003

    Application Number : 20030220000010

    Regulatory Info : Deregistered

    Registration Country : Sweden

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