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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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    Aurigene is a global leader in accelerating drug innovation through discovery, development & manufacturing.

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    Midas Pharma provides expertise in developing and supplying APIs, finished products, and intermediates.

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

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    Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.

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    Thioridazine

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    GLOBAL SALES INFORMATION

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

    ANALYTICAL

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    NOVARTIS

    Switzerland
    PharmaVenue
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    NOVARTIS

    Switzerland
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    PharmaVenue
    Not Confirmed
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    • WHO-GMP
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    RLD : No

    TE Code :

    THIORIDAZINE

    Brand Name : MELLARIL-S

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : EQ 25MG HYDROCHLORIDE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 17923

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    NOVARTIS

    Switzerland
    PharmaVenue
    Not Confirmed
    arrow

    NOVARTIS

    Switzerland
    arrow
    PharmaVenue
    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 Switzerland
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    Digital Content Digital Content

    RLD : No

    TE Code :

    THIORIDAZINE

    Brand Name : MELLARIL-S

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : EQ 100MG HYDROCHLORIDE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 17923

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF