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    Approved Drug Products containing MolPort-000-883-856 listed in the FDA Orange Book. Original Data : FDA Website

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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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    MolPort-000-883-856

    ACTIVE PHARMA INGREDIENTS

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    01

    GLAXOSMITHKLINE

    United Kingdom
    AAPS 2024
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    AAPS 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    AMPRENAVIR

    Brand Name : AGENERASE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 50MG

    Approval Date : 1999-04-15

    Application Number : 21007

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    02

    GLAXOSMITHKLINE

    United Kingdom
    AAPS 2024
    Not Confirmed
    arrow

    GLAXOSMITHKLINE

    United Kingdom
    arrow
    AAPS 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
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    RLD : No

    TE Code :

    AMPRENAVIR

    Brand Name : AGENERASE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

    Approval Date : 1999-04-15

    Application Number : 21007

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    03

    GLAXOSMITHKLINE

    United Kingdom
    AAPS 2024
    Not Confirmed
    arrow

    GLAXOSMITHKLINE

    United Kingdom
    arrow
    AAPS 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag United Kingdom
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : Yes

    TE Code :

    AMPRENAVIR

    Brand Name : AGENERASE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 15MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1999-04-15

    Application Number : 21039

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF