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

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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    pharmacompass-1-m-2026-01-12

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    Evonik Health Care is the innovation hub for leading life science companies

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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    pharmacompass-2-2026-02-09

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    Recordati

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    SUTIMLIMAB-JOME

    Brand Name : ENJAYMO

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1,100MG/22ML(50MG/ML)

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    Application Number : 761164

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    Registration Country : USA

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    Regulatory Info : Allowed

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    Brand Name : Enjaymo

    Dosage Form : Infusion Solution

    Dosage Strength : 1100mg/22ml

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    Approval Date : 21/06/2023

    Application Number : 68074

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    03

    Recordati Rare Diseases

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    Regulatory Info : Marketed

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    Brand Name : Enjaymo

    Dosage Form : Solution For Infusion

    Dosage Strength : 50mg/ml

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    Regulatory Info : Marketed

    Registration Country : Norway

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    04

    Recordati Rare Diseases

    U.S.A
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    Dosage Form : Solution For Infusion

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    Regulatory Info : Prescription

    Registration Country : Estonia

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    05

    Recordati Rare Diseases

    U.S.A
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    Recordati Rare Diseases

    U.S.A
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    Regulatory Info : Authorized

    Registration Country : Spain

    Sutimlimab

    Brand Name : Enjaymo

    Dosage Form : Infusion Solution

    Dosage Strength : 50MG

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    Approval Date : 29-12-2025

    Application Number : 1221687001

    Regulatory Info : Authorized

    Registration Country : Spain

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    06

    Recordati Rare Diseases

    U.S.A
    ASPEN
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    Recordati Rare Diseases

    U.S.A
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    • fda
    • EDQM
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    Regulatory Info : Prescription

    Registration Country : Denmark

    Sutimlimab

    Brand Name : Enjaymo

    Dosage Form : Infusion Solution

    Dosage Strength : 50mg/ml

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    Approval Date : 15-11-2022

    Application Number : 28106689921

    Regulatory Info : Prescription

    Registration Country : Denmark

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.