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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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    Daiichi Sankyo

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    European Pharma Congress
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    Sankyo Co Ltd

    Japan
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    European Pharma Congress
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    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 15051

    Submission : 2000-09-18

    Status : Inactive

    Type : II

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    Looking for Drug Master Files (DMF) for 15051 of Sankyo Co Ltd

    Looking for Drug Master Files (DMF) for 15051 of Sankyo Co Ltd 1

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    Sankyo Co Ltd, based in Japan, is a pharmaceutical company that stands out with its certifications from FDA.

    One of their notable products is CS-505 DRUG PRODUCT, with a corresponding US DMF Number 15051.

    Remarkably, this DMF maintains an Inactive status since its submission on September 18, 2000, 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.