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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Munit offers scalable GMP micronization and particle size engineering to enhance drug solubility, bioavailability, and performance.

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    Tocilizumab

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    01

    BIOGEN MA

    U.S.A
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    BIOGEN MA

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    RLD :

    TE Code :

    TOCILIZUMAB-BAVI

    Brand Name : TOFIDENCE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 80MG/4ML

    Approval Date :

    Application Number : 761354

    RX/OTC/DISCN :

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    TE Code :

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    02

    BIOGEN MA

    U.S.A
    AMWC Asia-TDAC
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    RLD :

    TE Code :

    TOCILIZUMAB-BAVI

    Brand Name : TOFIDENCE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 200MG/10ML

    Approval Date :

    Application Number : 761354

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    TE Code :

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    03

    BIOGEN MA

    U.S.A
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    RLD :

    TE Code :

    TOCILIZUMAB-BAVI

    Brand Name : TOFIDENCE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 400MG/20ML

    Approval Date :

    Application Number : 761354

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    04

    FRESENIUS KABI USA

    U.S.A
    AMWC Asia-TDAC
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    RLD :

    TE Code :

    TOCILIZUMAB-AAZG

    Brand Name : TYENNE

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : 80MG/4ML

    Approval Date :

    Application Number : 761275

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    05

    FRESENIUS KABI USA

    U.S.A
    AMWC Asia-TDAC
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    FRESENIUS KABI USA

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    AMWC Asia-TDAC
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    RLD :

    TE Code :

    TOCILIZUMAB-AAZG

    Brand Name : TYENNE

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : 200MG/10ML

    Approval Date :

    Application Number : 761275

    RX/OTC/DISCN :

    RLD :

    TE Code :

    blank

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    06

    FRESENIUS KABI USA

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    FRESENIUS KABI USA

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    AMWC Asia-TDAC
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    RLD :

    TE Code :

    TOCILIZUMAB-AAZG

    Brand Name : TYENNE

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : 400MG/20ML

    Approval Date :

    Application Number : 761275

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    07

    GENENTECH

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    AMWC Asia-TDAC
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    RLD :

    TE Code :

    TOCILIZUMAB

    Brand Name : ACTEMRA

    Dosage Form : INJECTABLE; INJECTION

    Dosage Strength : 80MG/4ML

    Approval Date :

    Application Number : 125276

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    08

    GENENTECH

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    GENENTECH

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
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    RLD :

    TE Code :

    TOCILIZUMAB

    Brand Name : ACTEMRA

    Dosage Form : INJECTABLE; INJECTION

    Dosage Strength : 200MG/10ML

    Approval Date :

    Application Number : 125276

    RX/OTC/DISCN :

    RLD :

    TE Code :

    blank

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    09

    GENENTECH

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    GENENTECH

    U.S.A
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    AMWC Asia-TDAC
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD :

    TE Code :

    TOCILIZUMAB

    Brand Name : ACTEMRA

    Dosage Form : INJECTABLE; INJECTION

    Dosage Strength : 400MG/20ML

    Approval Date :

    Application Number : 125276

    RX/OTC/DISCN :

    RLD :

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

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    10

    GENENTECH

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
    arrow

    GENENTECH

    U.S.A
    arrow
    AMWC Asia-TDAC
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD :

    TE Code :

    TOCILIZUMAB

    Brand Name : ACTEMRA

    Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 162MG/0.9ML

    Approval Date :

    Application Number : 125472

    RX/OTC/DISCN :

    RLD :

    TE Code :

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