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    List of All Manufacturers & Suppliers of Propyliodone Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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    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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    Propyliodone

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

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    GSK

    United Kingdom
    FNCE 2024
    Not Confirmed
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    GSK

    United Kingdom
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    FNCE 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    PROPYLIODONE

    Brand Name : DIONOSIL AQUEOUS

    Dosage Form : SUSPENSION;INTRATRACHEAL

    Dosage Strength : 50%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 9309

    Regulatory Info : DISCN

    Registration Country : USA

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    Product Web Link

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    02

    GSK

    United Kingdom
    FNCE 2024
    Not Confirmed
    arrow

    GSK

    United Kingdom
    arrow
    FNCE 2024
    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 United Kingdom
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    PROPYLIODONE

    Brand Name : DIONOSIL OILY

    Dosage Form : SUSPENSION;INTRATRACHEAL

    Dosage Strength : 60%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 9309

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF