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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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    KREITMAN ROBERT J MD

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    Kreitman Robert J Md

    U.S.A

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    RNA Leaders Europe
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    Kreitman Robert J Md

    U.S.A
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    RNA Leaders Europe
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    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 18630

    Submission : 1994-04-06

    Status : Active

    Type : II

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    Looking for Drug Master Files (DMF) for 18630 of Kreitman Robert J Md

    Looking for Drug Master Files (DMF) for 18630 of Kreitman Robert J Md 1

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    Kreitman Robert J Md, based in U.S.A, is a pharmaceutical company.

    One of their notable products is INTERLEUKIN-6 PSEUDOMONAS EXOTOXIN FUSION PROTEIN (HUMAN, RECOMBINANT, E. COLI), with a corresponding US DMF Number 18630.

    Remarkably, this DMF maintains an Active status since its submission on April 06, 1994, 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.