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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    01 4Global Blood Therapeutics

    02 2Pfizer Inc

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    01

    Global Blood Therapeutics

    U.S.A
    OTS 2025
    Not Confirmed
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    Global Blood Therapeutics

    U.S.A
    arrow
    OTS 2025
    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 : DISCN

    Registration Country : USA

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    Brand Name : OXBRYTA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2019-11-25

    Application Number : 213137

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Global Blood Therapeutics

    U.S.A
    OTS 2025
    Not Confirmed
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    Global Blood Therapeutics

    U.S.A
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    OTS 2025
    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 : DISCN

    Registration Country : USA

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    Brand Name : OXBRYTA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 300MG

    Packaging :

    Approval Date : 2022-10-14

    Application Number : 213137

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Global Blood Therapeutics

    U.S.A
    OTS 2025
    Not Confirmed
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    Global Blood Therapeutics

    U.S.A
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    OTS 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    VOXELOTOR

    Brand Name : OXBRYTA

    Dosage Form : TABLET, FOR SUSPENSION;ORAL

    Dosage Strength : 300MG

    Packaging :

    Approval Date : 2021-12-17

    Application Number : 216157

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Global Blood Therapeutics

    U.S.A
    OTS 2025
    Not Confirmed
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    Global Blood Therapeutics

    U.S.A
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    OTS 2025
    Not Confirmed
    • fda
    • EDQM
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    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 :

    Registration Country : USA

    VOXELOTOR

    Brand Name : OXBRYTA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Packaging :

    Approval Date :

    Application Number : 216157

    Regulatory Info :

    Registration Country : USA

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    05

    Pfizer Inc

    U.S.A
    OTS 2025
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    OTS 2025
    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 : Temporarily Withdrawn

    Registration Country : Sweden

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    Brand Name : Oxbryta

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500mg

    Packaging :

    Approval Date : 14/02/2022

    Application Number : 20201228000054

    Regulatory Info : Temporarily Withdrawn

    Registration Country : Sweden

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    06

    Pfizer Inc

    U.S.A
    OTS 2025
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    OTS 2025
    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 : Suspensed

    Registration Country : Spain

    Voxelotor

    Brand Name : Oxbryta

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2024-02-05

    Application Number : 1211622001

    Regulatory Info : Suspensed

    Registration Country : Spain

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