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    Approved Drug Products containing Methoxamine listed in the FDA Orange Book. Original Data : FDA Website

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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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    Methoxamine

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

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    GLAXOSMITHKLINE

    United Kingdom
    Discovery on Target
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    METHOXAMINE HYDROCHLORIDE

    Brand Name : VASOXYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

    Approval Date : 1982-01-01

    Application Number : 6772

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    02

    GLAXOSMITHKLINE

    United Kingdom
    Discovery on Target
    Not Confirmed
    arrow

    GLAXOSMITHKLINE

    United Kingdom
    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
    Flag United Kingdom
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    METHOXAMINE HYDROCHLORIDE

    Brand Name : VASOXYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Approval Date : 1982-01-01

    Application Number : 6772

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF