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    Approved Drug Products of Blue Earth Technology listed in the FDA Orange Book. Original Data : FDA Website

    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    01 1FLOTUFOLASTAT F-18 GALLIUM

    02 1FLUCICLOVINE F-18

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    01

    Brand Name : POSLUMA

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : POSLUMA

    U.S.A
    Discovery on Target
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    FLOTUFOLASTAT F-18 GALLIUM

    Blue Earth Technology

    Dosage Form : SOLUTION; INTRAVENOUS

    Proprietary Name : POSLUMA

    Dosage Strength : 25ML (8-158mCi/ML)

    Approval Date : 2023-05-25

    Application Number : 216023

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    Brand Name : AXUMIN

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : AXUMIN

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow
    • 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 U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : Yes

    TE Code :

    FLUCICLOVINE F-18

    Blue Earth Technology

    Dosage Form : SOLUTION; INTRAVENOUS

    Proprietary Name : AXUMIN

    Dosage Strength : 9-221mCi/ML

    Approval Date : 2016-05-27

    Application Number : 208054

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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