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    Brand Name : REMIFENTANIL HYDROCH...

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    Brand Name : REMIFENTANIL HYDROCH...

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    Regulatory Info : RX

    Registration Country : USA

    Remifentanil Hydrochloride

    Fresenius Kabi USA

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : REMIFENTANIL HYDROCHLORID...

    Dosage Strength : EQ 1MG BASE/VIAL

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    Approval Date : 2018-01-16

    Application Number : 206223

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : REMIFENTANIL HYDROCH...

    U.S.A
    AACR Annual meeting
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    Brand Name : REMIFENTANIL HYDROCH...

    U.S.A
    arrow
    AACR Annual meeting
    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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    Regulatory Info : RX

    Registration Country : USA

    Remifentanil Hydrochloride

    Fresenius Kabi USA

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : REMIFENTANIL HYDROCHLORID...

    Dosage Strength : EQ 2MG BASE/VIAL

    Packaging :

    Approval Date : 2018-01-16

    Application Number : 206223

    Regulatory Info : RX

    Registration Country : USA

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    03

    Brand Name : REMIFENTANIL HYDROCH...

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Brand Name : REMIFENTANIL HYDROCH...

    U.S.A
    arrow
    AACR Annual meeting
    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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    Flag U.S.A
    Virtual Booth Virtual Booth
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    Regulatory Info : RX

    Registration Country : USA

    Remifentanil Hydrochloride

    Fresenius Kabi USA

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : REMIFENTANIL HYDROCHLORID...

    Dosage Strength : EQ 5MG BASE/VIAL

    Packaging :

    Approval Date : 2018-01-16

    Application Number : 206223

    Regulatory Info : RX

    Registration Country : USA

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