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    List of All Manufacturers & Suppliers of Floxuridine Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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    Renejix: CDMO with expertise in small molecule oral dosage, delivery tech, and multi-modality manufacturing.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    xyz-pharma-m-2024-10-07

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    Ribobay has expertise in oligonucleotides from siRNA, Antisense Oligonucleotides, miRNAs, and aptamers & Oligonucleotides CXOs.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    xyz-pharma-m-2024-10-07

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    Floxuridine

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    DIGITAL CONTENT

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    01 1American Regent

    02 1Fresenius Kabi USA

    03 1Hikma Pharmaceuticals

    04 1Hospira, Inc.

    05 1Quad Pharma

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    01

    American Regent

    U.S.A
    AAPS 2024
    Not Confirmed
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    American Regent

    U.S.A
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    AAPS 2024
    Not Confirmed
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    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    FLOXURIDINE

    Brand Name : FLOXURIDINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500MG/VIAL

    Packaging :

    Approval Date : 2017-11-22

    Application Number : 203008

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Fresenius Kabi USA

    U.S.A
    AAPS 2024
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    AAPS 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    FLOXURIDINE

    Brand Name : FLOXURIDINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500MG/VIAL

    Packaging :

    Approval Date : 2001-02-22

    Application Number : 75837

    Regulatory Info : RX

    Registration Country : USA

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    03

    Hikma Pharmaceuticals

    United Kingdom
    AAPS 2024
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    AAPS 2024
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    FLOXURIDINE

    Brand Name : FLOXURIDINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500MG/VIAL

    Packaging :

    Approval Date : 2000-04-16

    Application Number : 75387

    Regulatory Info : RX

    Registration Country : USA

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    04

    Hospira, Inc.

    U.S.A
    AAPS 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AAPS 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    FLOXURIDINE

    Brand Name : FUDR

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 16929

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Quad Pharma

    South Africa
    AAPS 2024
    Not Confirmed
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    Quad Pharma

    South Africa
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    AAPS 2024
    Not Confirmed
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    Regulatory Info :

    Registration Country : USA

    FLOXURIDINE

    Brand Name : FLOXURIDINE

    Dosage Form : Injectable; Injection

    Dosage Strength : 500MG/VIAL

    Packaging :

    Approval Date :

    Application Number : 71055

    Regulatory Info :

    Registration Country : USA

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    Product Web Link

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