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    APOTEX

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    RLD :

    TE Code :

    Ruxolitinib

    Brand Name : Ruxolitinib

    Dosage Form : TABLET; ORAL

    Dosage Strength : 10MG

    Approval Date :

    Application Number : 219660

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    RLD :

    TE Code :

    Ruxolitinib

    Brand Name : Ruxolitinib

    Dosage Form : TABLET; ORAL

    Dosage Strength : 15MG

    Approval Date :

    Application Number : 219660

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    RLD :

    TE Code :

    Ruxolitinib

    Brand Name : Ruxolitinib

    Dosage Form : TABLET; ORAL

    Dosage Strength : 2MG

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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Brand Name : JAKAFI

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Approval Date : 2011-11-16

    Application Number : 202192

    RX/OTC/DISCN : RX

    RLD : Yes

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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Brand Name : JAKAFI

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2011-11-16

    Application Number : 202192

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    06

    INCYTE CORP

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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Brand Name : JAKAFI

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 15MG BASE

    Approval Date : 2011-11-16

    Application Number : 202192

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    INCYTE CORP

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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Brand Name : JAKAFI

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2011-11-16

    Application Number : 202192

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    08

    INCYTE CORP

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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Brand Name : JAKAFI

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Approval Date : 2011-11-16

    Application Number : 202192

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    09

    INCYTE CORP

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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Brand Name : OPZELURA

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : EQ 1.5% BASE

    Approval Date : 2021-09-21

    Application Number : 215309

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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