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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    Zilucoplan Sodium

    ACTIVE PHARMA INGREDIENTS

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    UCB Pharma S.A

    Belgium
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    UCB Pharma S.A

    Belgium
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    Regulatory Info : RX

    Registration Country : USA

    ZILUCOPLAN SODIUM

    Brand Name : ZILBRYSQ

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : EQ 16.6MG BASE/0.416ML (EQ 16.6MG BASE/0.416ML)

    Packaging :

    Approval Date : 2023-10-17

    Application Number : 216834

    Regulatory Info : RX

    Registration Country : USA

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    UCB Pharma S.A

    Belgium
    Antibody Engineering
    Not Confirmed
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    UCB Pharma S.A

    Belgium
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    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    ZILUCOPLAN SODIUM

    Brand Name : ZILBRYSQ

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : EQ 23MG BASE/0.574ML (EQ 23MG BASE/0.574ML)

    Packaging :

    Approval Date : 2023-10-17

    Application Number : 216834

    Regulatory Info : RX

    Registration Country : USA

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    03

    UCB Pharma S.A

    Belgium
    Antibody Engineering
    Not Confirmed
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    UCB Pharma S.A

    Belgium
    arrow
    Antibody Engineering
    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.
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    Regulatory Info : RX

    Registration Country : USA

    ZILUCOPLAN SODIUM

    Brand Name : ZILBRYSQ

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : EQ 32.4MG BASE/0.81ML (EQ 32.4 BASE/0.81ML)

    Packaging :

    Approval Date : 2023-10-17

    Application Number : 216834

    Regulatory Info : RX

    Registration Country : USA

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