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    List of Drug Master Files (DMF) for 17838 Active Pharmaceutical Ingredient (API) submitted to the U.S. FDA. Original Data : FDA Website

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    Bioiberica

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    01 Bioiberica (1)

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    01 HEPARIN SODIUM (1)

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    BIOIBERICA SAU

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    Virtual BoothBioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
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    HEPARIN SODIUM

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    17838
    Active
    2004-11-03
    Complete
    2013-05-09
    2013-04-26
    II
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    Looking for Drug Master Files (DMF) for 17838 of Bioiberica Sau

    Looking for Drug Master Files (DMF) for 17838 of Bioiberica Sau 1

    20

    Bioiberica Sau, based in Spain, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    They are recognized for Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.

    One of their notable products is HEPARIN SODIUM, with a corresponding US DMF Number 17838.

    Remarkably, this DMF maintains an Active status since its submission on November 03, 2004, highlighting commitment to regulatory compliance.

    Their GDUFA DMF Review was successfully complete, with a review date of May 09, 2013, and payment made on April 26, 2013, indicating their dedication to facilitating drug approvals, Categorized as Type II

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