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    01 3FRESENIUS KABI USA

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    03 3MYLAN INSTITUTIONAL

    04 3NIVAGEN PHARMS INC

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    01

    FRESENIUS KABI USA

    U.S.A
    CPhI India 2024
    Not Confirmed
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    FRESENIUS KABI USA

    U.S.A
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    CPhI India 2024
    Not Confirmed
    • fda
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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
    CPhI India 2024
    Not Confirmed
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    FRESENIUS KABI USA

    U.S.A
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    CPhI India 2024
    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 : 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
    CPhI India 2024
    Not Confirmed
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    FRESENIUS KABI USA

    U.S.A
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    CPhI India 2024
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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
    CPhI India 2024
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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
    CPhI India 2024
    Not Confirmed
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    HIKMA

    United Kingdom
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    CPhI India 2024
    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
    CPhI India 2024
    Not Confirmed
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    HIKMA

    United Kingdom
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    CPhI India 2024
    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 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
    CPhI India 2024
    Not Confirmed
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    NIVAGEN PHARMS INC

    U.S.A
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    CPhI India 2024
    Not Confirmed
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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
    CPhI India 2024
    Not Confirmed
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    MYLAN INSTITUTIONAL

    U.S.A
    arrow
    CPhI India 2024
    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
    CPhI India 2024
    Not Confirmed
    arrow

    MYLAN INSTITUTIONAL

    U.S.A
    arrow
    CPhI India 2024
    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
    CPhI India 2024
    Not Confirmed
    arrow

    MYLAN INSTITUTIONAL

    U.S.A
    arrow
    CPhI India 2024
    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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    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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