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    Alkem Laboratories

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    DROXIDOPA

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    DROXIDOPA

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    Approval Date : 2021-04-28

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    10

    H. Lundbeck AS

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    DROXIDOPA

    Brand Name : NORTHERA

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    Approval Date : 2014-02-18

    Application Number : 203202

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    Hikma Pharmaceuticals

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    DROXIDOPA

    Brand Name : DROXIDOPA

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    Approval Date : 2021-02-18

    Application Number : 212835

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    14

    Hikma Pharmaceuticals

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    Brand Name : DROXIDOPA

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    MSN Laboratories

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    Pfizer Inc

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    Approval Date : 2021-02-18

    Application Number : 211652

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    Teva Pharmaceutical Industries

    Israel
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    Approval Date : 2021-02-18

    Application Number : 213162

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    Upsher-Smith Laboratories

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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    DROXIDOPA

    Brand Name : DROXIDOPA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 2021-02-18

    Application Number : 213661

    Regulatory Info : DISCN

    Registration Country : USA

    blank

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    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    26

    Upsher-Smith Laboratories

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Upsher-Smith Laboratories

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    DROXIDOPA

    Brand Name : DROXIDOPA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 2021-02-18

    Application Number : 213661

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    27

    Upsher-Smith Laboratories

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Upsher-Smith Laboratories

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    DROXIDOPA

    Brand Name : DROXIDOPA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 300MG

    Packaging :

    Approval Date : 2021-02-18

    Application Number : 213661

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    28

    Zydus Pharmaceuticals

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Zydus Pharmaceuticals

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    DROXIDOPA

    Brand Name : DROXIDOPA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 2021-02-18

    Application Number : 211818

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    29

    Zydus Pharmaceuticals

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Zydus Pharmaceuticals

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    DROXIDOPA

    Brand Name : DROXIDOPA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 2021-02-18

    Application Number : 211818

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    30

    Zydus Pharmaceuticals

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Zydus Pharmaceuticals

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    DROXIDOPA

    Brand Name : DROXIDOPA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 300MG

    Packaging :

    Approval Date : 2021-02-18

    Application Number : 211818

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF