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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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    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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    Levena Biopharma

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    Levena (suzhou) Biopharma Co Ltd

    China
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    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 37905

    Submission : 2022-12-30

    Status : Active

    Type : II

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    Looking for Drug Master Files (DMF) for 37905 of Levena (suzhou) Biopharma Co Ltd

    Looking for Drug Master Files (DMF) for 37905 of Levena (suzhou) Biopharma Co Ltd 1

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    Levena (suzhou) Biopharma Co Ltd, based in China, is a pharmaceutical company.

    One of their notable products is LND1030 (EXATECAN MESYLATE), with a corresponding US DMF Number 37905.

    Remarkably, this DMF maintains an Active status since its submission on December 30, 2022, 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.