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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

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    USP reference standards; highly characterized specimens of drug substances, impurities, excipients, degradation products & more.

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

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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    Guizhou Utide Biotechnology Co., Ltd. - Specialized GMP manufacturing for next-generation GLP-1 peptide APIs.

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    IBA MOLECULAR NORTH AMERICA INC

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    Sofie Co Dba Sofie

    U.S.A

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    Sofie Co Dba Sofie

    U.S.A
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    BePharma
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    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 25370

    Submission : 2011-10-03

    Status : Active

    Type : II

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    Looking for Drug Master Files (DMF) for 25370 of Sofie Co Dba Sofie

    Looking for Drug Master Files (DMF) for 25370 of Sofie Co Dba Sofie 1

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    Sofie Co Dba Sofie, based in U.S.A, is a pharmaceutical company.

    One of their notable products is 3'-DEOXY-3'-[18F]FLUOROTHYMIDINE, with a corresponding US DMF Number 25370.

    Remarkably, this DMF maintains an Active status since its submission on October 03, 2011, highlighting commitment to regulatory compliance.

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.