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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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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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    xyz-pharma-m-2025-03-24

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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.

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    xyz-pharma-m-2025-03-17

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    Fruquintinib

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    FINISHED DOSAGE FORMULATIONS

    DIGITAL CONTENT

    PATENTS & EXCLUSIVITIES

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    $ API Ref.Price (USD/KG) : 7,089Xls

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    01 2Takeda Pharmaceutical

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    Takeda Pharmaceutical

    Japan
    Immuno-Oncology 360
    Not Confirmed
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    Takeda Pharmaceutical

    Japan
    arrow
    Immuno-Oncology 360
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    FRUQUINTINIB

    Brand Name : FRUZAQLA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 2023-11-08

    Application Number : 217564

    Regulatory Info : RX

    Registration Country : USA

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    02

    Takeda Pharmaceutical

    Japan
    Immuno-Oncology 360
    Not Confirmed
    arrow

    Takeda Pharmaceutical

    Japan
    arrow
    Immuno-Oncology 360
    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 Japan
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    FRUQUINTINIB

    Brand Name : FRUZAQLA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2023-11-08

    Application Number : 217564

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF