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    Approved Drug Products containing MolPort-001-756-344 listed in the FDA Orange Book. Original Data : FDA Website

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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    FAMAR CDMO- From early development to commercial manufacturing.

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    xyz-pharma-m-2024-09-09

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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    Veranova: A CDMO that manages complexity with confidence.

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    xyz-pharma-m-2024-09-09

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    MolPort-001-756-344

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    01 1BRACCO

    02 1JUBILANT

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    01

    BRACCO

    Italy
    Boulder Peptide 2024
    Not Confirmed
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    BRACCO

    Italy
    arrow
    Boulder Peptide 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.
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    RLD : No

    TE Code :

    RUBIDIUM CHLORIDE RB-82

    Brand Name : CARDIOGEN-82

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : N/A

    Approval Date : 1989-12-29

    Application Number : 19414

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

    blank

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    02

    JUBILANT

    India
    Boulder Peptide 2024
    Not Confirmed
    arrow

    JUBILANT

    India
    arrow
    Boulder Peptide 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 India
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    RUBIDIUM CHLORIDE RB-82

    Brand Name : RUBY-FILL

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : N/A

    Approval Date : 2016-09-30

    Application Number : 202153

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF