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    Aspen Pharmacare Holdings

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    Brand Name : Ultiva 2 mg

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    Orion Corporation

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    remifentanilhydroklorid

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    Dosage Strength : EQ 1MG BASE/VIAL

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    Approval Date : 2018-01-16

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    Fresenius Kabi USA

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    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 2018-01-16

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    Fresenius Kabi USA

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    Dosage Strength : EQ 5MG BASE/VIAL

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    Approval Date : 2018-01-16

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    12

    Hikma Pharmaceuticals

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    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/VIAL

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    Approval Date : 2020-10-13

    Application Number : 210594

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    Registration Country : USA

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    13

    Hikma Pharmaceuticals

    United Kingdom
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    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2MG BASE/VIAL

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    Approval Date : 2020-10-13

    Application Number : 210594

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    Registration Country : USA

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    14

    Hikma Pharmaceuticals

    United Kingdom
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    REMIFENTANIL HYDROCHLORIDE

    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/VIAL

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    Approval Date : 2020-10-13

    Application Number : 210594

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    Registration Country : USA

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    15

    Nivagen

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    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/VIAL

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    Approval Date : 2024-06-28

    Application Number : 215635

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    Registration Country : USA

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    16

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    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2MG BASE/VIAL

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    Approval Date : 2024-06-28

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    17

    Nivagen

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    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/VIAL

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    Approval Date : 2024-06-28

    Application Number : 215635

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    18

    Viatris

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    REMIFENTANIL HYDROCHLORIDE

    Brand Name : ULTIVA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/VIAL

    Packaging :

    Approval Date : 1996-07-12

    Application Number : 20630

    Regulatory Info : RX

    Registration Country : USA

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    19

    Viatris

    U.S.A
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    Brand Name : ULTIVA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2MG BASE/VIAL

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    Approval Date : 1996-07-12

    Application Number : 20630

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    Registration Country : USA

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    Viatris

    U.S.A
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    Brand Name : ULTIVA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/VIAL

    Packaging :

    Approval Date : 1996-07-12

    Application Number : 20630

    Regulatory Info : RX

    Registration Country : USA

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