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    01 3FRESENIUS KABI USA

    02 3HIKMA

    03 3MYLAN INSTITUTIONAL

    04 3NIVAGEN PHARMS INC

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    01

    FRESENIUS KABI USA

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    FRESENIUS KABI USA

    U.S.A
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    RLD : No

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/VIAL

    Approval Date : 2018-01-16

    Application Number : 206223

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    FRESENIUS KABI USA

    U.S.A
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    FRESENIUS KABI USA

    U.S.A
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    Pharma, Lab & Chemical Expo
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    RLD : No

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2MG BASE/VIAL

    Approval Date : 2018-01-16

    Application Number : 206223

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    FRESENIUS KABI USA

    U.S.A
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    FRESENIUS KABI USA

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    RLD : No

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/VIAL

    Approval Date : 2018-01-16

    Application Number : 206223

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    04

    HIKMA

    United Kingdom
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    RLD : No

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/VIAL

    Approval Date : 2020-10-13

    Application Number : 210594

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    05

    HIKMA

    United Kingdom
    Pharma, Lab & Chemical Expo
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    HIKMA

    United Kingdom
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    RLD : No

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2MG BASE/VIAL

    Approval Date : 2020-10-13

    Application Number : 210594

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    06

    HIKMA

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    HIKMA

    United Kingdom
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Virtual Booth Virtual Booth
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    RLD : No

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/VIAL

    Approval Date : 2020-10-13

    Application Number : 210594

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    07

    NIVAGEN PHARMS INC

    U.S.A
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    NIVAGEN PHARMS INC

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    RLD : No

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : REMIFENTANIL HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/VIAL

    Approval Date : 2024-06-28

    Application Number : 215635

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    08

    MYLAN INSTITUTIONAL

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    MYLAN INSTITUTIONAL

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Flag U.S.A
    Virtual Booth Virtual Booth
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    RLD : Yes

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : ULTIVA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/VIAL

    Approval Date : 1996-07-12

    Application Number : 20630

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    09

    MYLAN INSTITUTIONAL

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    MYLAN INSTITUTIONAL

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : Yes

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : ULTIVA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2MG BASE/VIAL

    Approval Date : 1996-07-12

    Application Number : 20630

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    10

    MYLAN INSTITUTIONAL

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    MYLAN INSTITUTIONAL

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    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
    Digital Content Digital Content

    RLD : Yes

    TE Code : AP

    REMIFENTANIL HYDROCHLORIDE

    Brand Name : ULTIVA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/VIAL

    Approval Date : 1996-07-12

    Application Number : 20630

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

    blank

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    Product Web Link

    Virtual Booth

    Digital Content

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    Corporate PDF