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    List of All Manufacturers & Suppliers for 7842 Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    FAMAR CDMO- From early development to commercial manufacturing.

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    xyz-pharma-m-2024-09-09

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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    Veranova: A CDMO that manages complexity with confidence.

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    xyz-pharma-m-2024-09-09

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    DAVIS AND GECK

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    FINISHED DOSAGE FORMULATIONS

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    01 2GALLAMINE TRIETHIODIDE

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    01

    Brand Name : FLAXEDIL

    U.S.A
    Boulder Peptide 2024
    Not Confirmed
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    Brand Name : FLAXEDIL

    U.S.A
    arrow
    Boulder Peptide 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    Gallamine Triethiodide

    DAVIS AND GECK

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : FLAXEDIL

    Dosage Strength : 100MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 7842

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Brand Name : FLAXEDIL

    U.S.A
    Boulder Peptide 2024
    Not Confirmed
    arrow

    Brand Name : FLAXEDIL

    U.S.A
    arrow
    Boulder Peptide 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 U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    Gallamine Triethiodide

    DAVIS AND GECK

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : FLAXEDIL

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 7842

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Market
    Place