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    Approved Drug Products containing Prestwick3_001037 listed in the FDA Orange Book. Original Data : FDA Website

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    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    xyz-pharma-m-2024-09-09

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    Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    xyz-pharma-m-2024-09-09

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    Prestwick3_001037

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    DIGITAL CONTENT

    PATENTS & EXCLUSIVITIES

    REF. STANDARDS & IMPURITIES

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    01 2ROCHE

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    01

    ROCHE

    Switzerland
    Formnext Forum
    Not Confirmed
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    ROCHE

    Switzerland
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    Formnext Forum
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    ZALCITABINE

    Brand Name : HIVID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.375MG

    Approval Date : 1992-06-19

    Application Number : 20199

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

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    Website

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    02

    ROCHE

    Switzerland
    Formnext Forum
    Not Confirmed
    arrow

    ROCHE

    Switzerland
    arrow
    Formnext Forum
    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
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    ZALCITABINE

    Brand Name : HIVID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.75MG

    Approval Date : 1992-06-19

    Application Number : 20199

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF