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    Remifentanil Hydrochloride

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    01 5Aspen Pharmacare Holdings

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    06 4Cristalia Produtos Quimicos Farma. Ltda

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    Aspen Pharmacare Holdings

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    Remifentanil

    Brand Name : Fortiva 1mg

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    remifentanilhydroklorid

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    Remifentanil

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    Remifentanil

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    Orion Corporation

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    remifentanilhydroklorid

    Brand Name : Remifentanil Orion

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    Cristalia Produtos Quimicos Farma. ...

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    remifentanil hydrochloride

    Brand Name : REMIFENTANIL HYDROCHLORIDE

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    Cristalia Produtos Quimicos Farma. ...

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    Brand Name : REMIFENTANIL HYDROCHLORIDE

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    Packaging : 5 VIALS

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    Cristalia Produtos Quimicos Farma. ...

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    Brand Name : REMIFENTANIL HYDROCHLORIDE

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    Cristalia Produtos Quimicos Farma. ...

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    13

    Fresenius Kabi USA

    U.S.A
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    REMIFENTANIL HYDROCHLORIDE

    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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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    14

    Fresenius Kabi USA

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    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2MG BASE/VIAL

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    Approval Date : 2018-01-16

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    Fresenius Kabi USA

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    Brand Name : REMIFENTANIL HYDROCHLORIDE

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    Dosage Strength : EQ 5MG BASE/VIAL

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    Approval Date : 2018-01-16

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    Hanlim Pharmaceuticals Inc

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    Brand Name : ULTIAN

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    Hanlim Pharmaceuticals Inc

    South Korea
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    Hanlim Pharmaceuticals Inc

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    Hikma Pharmaceuticals

    United Kingdom
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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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    Hikma Pharmaceuticals

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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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    Hikma Pharmaceuticals

    United Kingdom
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    Dosage Strength : EQ 5MG BASE/VIAL

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    Approval Date : 2020-10-13

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    Nivagen

    U.S.A
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    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/VIAL

    Packaging :

    Approval Date : 2024-06-28

    Application Number : 215635

    Regulatory Info : RX

    Registration Country : USA

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    Nivagen

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    Approval Date : 2024-06-28

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    Nivagen

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    Dosage Strength : EQ 5MG BASE/VIAL

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    Approval Date : 2024-06-28

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    Sandoz B2B

    Switzerland
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    remifentanilhydroklorid

    Brand Name : Remifentanil Sandoz

    Dosage Form : PULVER TILL KONCENTRAT TILL INJEKTIONS-

    Dosage Strength : 2 MG

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    Registration Country : Sweden

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    Sandoz B2B

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    remifentanilhydroklorid

    Brand Name : Remifentanil Sandoz

    Dosage Form : PULVER TILL KONCENTRAT TILL INJEKTIONS-

    Dosage Strength : 1 MG

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    Registration Country : Sweden

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    Sandoz B2B

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    remifentanilhydroklorid

    Brand Name : Remifentanil Sandoz

    Dosage Form : PULVER TILL KONCENTRAT TILL INJEKTIONS-

    Dosage Strength : 5 MG

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    Registration Country : Sweden

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    Viatris

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    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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    Viatris

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : ULTIVA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2MG BASE/VIAL

    Packaging :

    Approval Date : 1996-07-12

    Application Number : 20630

    Regulatory Info : RX

    Registration Country : USA

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    Viatris

    U.S.A
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    U.S.A
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    Regulatory Info : RX

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    REMIFENTANIL HYDROCHLORIDE

    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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