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    01 3ANAKINRA

    02 5NITISINONE

    03 1PACRITINIB CITRATE

    04 1PALIFERMIN

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    Brand Name : KINERET

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    TE Code :

    ANAKINRA

    Swedish Orphan Biovitrum AB

    Dosage Form : VIAL; SUBCUTANEOUS

    Proprietary Name : KINERET

    Dosage Strength : 10MIU/VIAL

    Approval Date :

    Application Number : 103950

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    RLD :

    TE Code :

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    Brand Name : KINERET

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    RLD :

    TE Code :

    ANAKINRA

    Swedish Orphan Biovitrum AB

    Dosage Form : VIAL; SUBCUTANEOUS

    Proprietary Name : KINERET

    Dosage Strength : 18MIU/VIAL

    Approval Date :

    Application Number : 103950

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    ANAKINRA

    Swedish Orphan Biovitrum AB

    Dosage Form : VIAL; SUBCUTANEOUS

    Proprietary Name : KINERET

    Dosage Strength : 25MIU/VIAL

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    Swedish Orphan Biovitrum AB

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : ORFADIN

    Dosage Strength : 2MG

    Approval Date : 2002-01-18

    Application Number : 21232

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    RLD : Yes

    TE Code : AB

    NITISINONE

    Swedish Orphan Biovitrum AB

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : ORFADIN

    Dosage Strength : 5MG

    Approval Date : 2002-01-18

    Application Number : 21232

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    Brand Name : ORFADIN

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    euroPLX 86 Munich
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    RLD : Yes

    TE Code : AB

    NITISINONE

    Swedish Orphan Biovitrum AB

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : ORFADIN

    Dosage Strength : 10MG

    Approval Date : 2002-01-18

    Application Number : 21232

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    07

    Brand Name : ORFADIN

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    euroPLX 86 Munich
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    RLD : Yes

    TE Code : AB

    NITISINONE

    Swedish Orphan Biovitrum AB

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : ORFADIN

    Dosage Strength : 20MG

    Approval Date : 2016-06-13

    Application Number : 21232

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    Brand Name : ORFADIN

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    euroPLX 86 Munich
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    RLD : Yes

    TE Code :

    NITISINONE

    Swedish Orphan Biovitrum AB

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : ORFADIN

    Dosage Strength : 4MG/ML

    Approval Date : 2016-04-22

    Application Number : 206356

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    Brand Name : VONJO

    U.S.A
    euroPLX 86 Munich
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    RLD : Yes

    TE Code :

    PACRITINIB CITRATE

    CTI BioPharma Corp

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : VONJO

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2022-02-28

    Application Number : 208712

    RX/OTC/DISCN : RX

    RLD : Yes

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    Brand Name : KEPIVANCE

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    euroPLX 86 Munich
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    RLD :

    TE Code :

    PALIFERMIN

    Swedish Orphan Biovitrum AB

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : KEPIVANCE

    Dosage Strength : 60MCG/KG/DAY

    Approval Date :

    Application Number : 125103

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    RLD :

    TE Code :

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