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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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    Xiamen SINOPEG Biotech

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    Xiamen Sinopeg Biotech Co Ltd

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    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 31760

    Submission : 2017-04-20

    Status : Active

    Type : II

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    Looking for Drug Master Files (DMF) for 31760 of Xiamen Sinopeg Biotech Co Ltd

    Looking for Drug Master Files (DMF) for 31760 of Xiamen Sinopeg Biotech Co Ltd 1

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    Xiamen Sinopeg Biotech Co Ltd, based in China, is a pharmaceutical company that stands out with its certifications from FDA.

    One of their notable products is METHOXYPOLY (ETHYLENE GLYCOL) SUCCINIMIDYL CARBONATE 5K, with a corresponding US DMF Number 31760.

    Remarkably, this DMF maintains an Active status since its submission on April 20, 2017, 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.