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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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    Teijin Pharma

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    BePharma
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    Teijin Pharma Ltd

    Japan
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    BePharma
    Not Confirmed

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 34225

    Submission : 2019-11-01

    Status : Active

    Type : II

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    Looking for Drug Master Files (DMF) for 34225 of Teijin Pharma Ltd

    Looking for Drug Master Files (DMF) for 34225 of Teijin Pharma Ltd 1

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    Teijin Pharma Ltd, based in Japan, is a pharmaceutical company.

    One of their notable products is TEI-R04969 DRUG SUBSTANCE, with a corresponding US DMF Number 34225.

    Remarkably, this DMF maintains an Active status since its submission on November 01, 2019, 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.