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    FAMAR CDMO- From early development to commercial manufacturing.

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    Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.

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

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    Together we can improve the quality of life

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    Brand Name : Tevimbra

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    Regulatory Info : Approved

    Registration Country : Sweden

    Tislelizumab

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    Dosage Form : Concentrate For Solution For I...

    Dosage Strength : 100mg

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    Brand Name : Tevimbra

    Approval Date : 15/09/2023

    Application Number : 20220304000085

    Regulatory Info : Approved

    Registration Country : Sweden

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    Brand Name : Tizveni

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    Regulatory Info : Deregistered

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    Tislelizumab

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    Brand Name : Tizveni

    Approval Date : 19/04/2024

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    Regulatory Info : Allowed

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    Tislelizumabum

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    Dosage Strength : 100mg/10ml

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    Brand Name : Tevimbra

    Approval Date : 11/04/2024

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    Regulatory Info : Marketed

    Registration Country : Norway

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    Regulatory Info : Marketed

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    Zanubrutinib

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    Dosage Form : Capsule

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    Brand Name : Brukinsa

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    Regulatory Info : Prescription

    Registration Country : Estonia

    Tislelizumab

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    Dosage Form : Concentrate For Solution For I...

    Dosage Strength : 100mg/10ml

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    Brand Name : Brukinsa

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    Regulatory Info : Prescription

    Registration Country : Estonia

    Zanubrutinib

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    Dosage Form : Capsule

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    Brand Name : Brukinsa

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    Brand Name : Brukinsa

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    Regulatory Info : Authorized

    Registration Country : Spain

    Zanubrutinib

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    Dosage Form : Hard Capsule

    Dosage Strength : 80MG

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    Brand Name : Brukinsa

    Approval Date : 14-12-2021

    Application Number : 1211576001

    Regulatory Info : Authorized

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    Brand Name : Tevimbra

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    Regulatory Info : Authorized

    Registration Country : Spain

    Tisselizumab

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    Dosage Form : Concentrate For Infusion Solut...

    Dosage Strength : 100MG

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    Brand Name : Tevimbra

    Approval Date : 26-07-2024

    Application Number : 1231758001

    Regulatory Info : Authorized

    Registration Country : Spain

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    Brand Name : Brukinsa

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    Regulatory Info : Authorized

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    Zanubrutinib

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    Dosage Form : Hard Capsule

    Dosage Strength : 80MG

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    Brand Name : Brukinsa

    Approval Date : 03-09-2025

    Application Number : 1211576001IP

    Regulatory Info : Authorized

    Registration Country : Spain

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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.