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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    xyz-pharma-m-2024-10-07

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    ATNAHS PHARMA UK LIMITED

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    Brand Name : NAPROSYN

    United Kingdom
    Pharma, Lab & Chemical Expo
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    Brand Name : NAPROSYN

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    RLD : Yes

    TE Code :

    NAPROXEN

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROSYN

    Dosage Strength : 250MG

    Approval Date : 1982-01-01

    Application Number : 17581

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    Brand Name : NAPROSYN

    United Kingdom
    Pharma, Lab & Chemical Expo
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    Brand Name : NAPROSYN

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    NAPROXEN

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROSYN

    Dosage Strength : 375MG

    Approval Date : 1982-01-01

    Application Number : 17581

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    03

    Brand Name : NAPROSYN

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Brand Name : NAPROSYN

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow
    • 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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    RLD : Yes

    TE Code : AB

    NAPROXEN

    ATNAHS PHARMA UK LIMITED

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROSYN

    Dosage Strength : 500MG

    Approval Date : 1982-04-15

    Application Number : 17581

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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