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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
    Pharmtech & Ingredients
    Not Confirmed
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    FRESENIUS KABI USA

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
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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
    Pharmtech & Ingredients
    Not Confirmed
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    FRESENIUS KABI USA

    U.S.A
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    Pharmtech & Ingredients
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    • fda
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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
    Pharmtech & Ingredients
    Not Confirmed
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    FRESENIUS KABI USA

    U.S.A
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    Pharmtech & Ingredients
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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
    Pharmtech & Ingredients
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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 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
    Pharmtech & Ingredients
    Not Confirmed
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    HIKMA

    United Kingdom
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    Pharmtech & Ingredients
    Not Confirmed
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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
    Pharmtech & Ingredients
    Not Confirmed
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    HIKMA

    United Kingdom
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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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
    Pharmtech & Ingredients
    Not Confirmed
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    NIVAGEN PHARMS INC

    U.S.A
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    Pharmtech & Ingredients
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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
    Pharmtech & Ingredients
    Not Confirmed
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    MYLAN INSTITUTIONAL

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    MYLAN INSTITUTIONAL

    U.S.A
    arrow
    Pharmtech & Ingredients
    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
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    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
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    MYLAN INSTITUTIONAL

    U.S.A
    arrow
    Pharmtech & Ingredients
    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
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    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

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF