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    UCB INC

    Belgium
    Pharma, Lab & Chemical Expo
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    UCB INC

    Belgium
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    RLD : Yes

    TE Code :

    ROTIGOTINE

    Brand Name : NEUPRO

    Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

    Dosage Strength : 2MG/24HR

    Approval Date : 2007-05-09

    Application Number : 21829

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    UCB INC

    Belgium
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    UCB INC

    Belgium
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    RLD : Yes

    TE Code :

    ROTIGOTINE

    Brand Name : NEUPRO

    Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

    Dosage Strength : 4MG/24HR

    Approval Date : 2007-05-09

    Application Number : 21829

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    UCB INC

    Belgium
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    UCB INC

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    RLD : Yes

    TE Code :

    ROTIGOTINE

    Brand Name : NEUPRO

    Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

    Dosage Strength : 6MG/24HR

    Approval Date : 2007-05-09

    Application Number : 21829

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    UCB INC

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    RLD : Yes

    TE Code :

    ROTIGOTINE

    Brand Name : NEUPRO

    Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

    Dosage Strength : 1MG/24HR

    Approval Date : 2012-04-02

    Application Number : 21829

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    05

    UCB INC

    Belgium
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    UCB INC

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    Pharma, Lab & Chemical Expo
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    • fda
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    RLD : Yes

    TE Code :

    ROTIGOTINE

    Brand Name : NEUPRO

    Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

    Dosage Strength : 3MG/24HR

    Approval Date : 2012-04-02

    Application Number : 21829

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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    06

    UCB INC

    Belgium
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    UCB INC

    Belgium
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Flag Belgium
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    RLD : Yes

    TE Code :

    ROTIGOTINE

    Brand Name : NEUPRO

    Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

    Dosage Strength : 8MG/24HR

    Approval Date : 2012-04-02

    Application Number : 21829

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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