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    Amivas's list of EU CTD Dossiers, Marketing Authorizations, In, Out Licensing Opportunities & Finished Dosage Formulations aggregated by PharmaCompass

    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Bora Pharmaceuticals- Making success more certain.

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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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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    Amivas

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    DIGITAL CONTENT

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    FINISHED DOSAGE FORMULATIONS

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    01

    Brand Name : Artesunate Amivas

    U.S.A
    Discovery on Target
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    Brand Name : Artesunate Amivas

    U.S.A
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    Discovery on Target
    Not Confirmed
    • fda
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    • WHO-GMP
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    Regulatory Info :

    Registration Country : Norway

    Artesunat

    Amivas

    Dosage Form : Powder and liquid for so...

    Brand Name : Artesunate Amivas

    Dosage Strength : 110 mg

    Packaging : Vials

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Norway

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    02

    Brand Name : ARTESUNATE

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    Brand Name : ARTESUNATE

    U.S.A
    arrow
    Discovery on Target
    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
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    Regulatory Info : RX

    Registration Country : USA

    ARTESUNATE

    Amivas

    Dosage Form : POWDER;INTRAVENOUS

    Brand Name : ARTESUNATE

    Dosage Strength : 110MG/VIAL

    Packaging :

    Approval Date : 2020-05-26

    Application Number : 213036

    Regulatory Info : RX

    Registration Country : USA

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