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    List of All Manufacturers & Suppliers of Methdilazine 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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    Methdilazine

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    REF. STANDARDS & IMPURITIES

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    01 1Actavis Inc

    02 3Bristol Myers Squibb

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    01

    Actavis Inc

    Ireland
    Discovery on Target
    Not Confirmed
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    Actavis Inc

    Ireland
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    METHDILAZINE HYDROCHLORIDE

    Brand Name : METHDILAZINE HYDROCHLORIDE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 4MG/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 87122

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Bristol Myers Squibb

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    Bristol Myers Squibb

    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.
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    Regulatory Info : DISCN

    Registration Country : USA

    METHDILAZINE HYDROCHLORIDE

    Brand Name : TACARYL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 8MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11950

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    03

    Bristol Myers Squibb

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    Bristol Myers Squibb

    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.
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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    METHDILAZINE HYDROCHLORIDE

    Brand Name : TACARYL

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 4MG/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11950

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    04

    Bristol Myers Squibb

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    Bristol Myers Squibb

    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
    Flag U.S.A
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    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    METHDILAZINE

    Brand Name : TACARYL

    Dosage Form : TABLET, CHEWABLE;ORAL

    Dosage Strength : 3.6MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11950

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF