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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    ScinoPharm Taiwan, Ltd

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    01 1BENZPHETAMINE HYDROCHLORIDE

    02 1BORTEZOMIB

    03 4FONDAPARINUX SODIUM

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    Brand Name : BENZPHETAMINE HYDROC...

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    Regulatory Info : DISCN

    Registration Country : USA

    BENZPHETAMINE HYDROCHLORIDE

    ScinoPharm Taiwan, Ltd

    Dosage Form : TABLET;ORAL

    Brand Name : BENZPHETAMINE HYDROCHLORI...

    Dosage Strength : 50MG

    Packaging :

    Approval Date : 2006-04-17

    Application Number : 40578

    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : BORTEZOMIB

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    Regulatory Info : DISCN

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    BORTEZOMIB

    ScinoPharm Taiwan, Ltd

    Dosage Form : INJECTABLE;INTRAVENOUS, ...

    Brand Name : BORTEZOMIB

    Dosage Strength : 3.5MG/VIAL

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    Approval Date : 2023-09-26

    Application Number : 216912

    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : FONDAPARINUX SODIUM

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    Regulatory Info : RX

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    FONDAPARINUX SODIUM

    ScinoPharm Taiwan, Ltd

    Dosage Form : INJECTABLE;SUBCUTANEOUS

    Brand Name : FONDAPARINUX SODIUM

    Dosage Strength : 2.5MG/0.5ML

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    Approval Date : 2018-11-14

    Application Number : 208615

    Regulatory Info : RX

    Registration Country : USA

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    FONDAPARINUX SODIUM

    ScinoPharm Taiwan, Ltd

    Dosage Form : INJECTABLE;SUBCUTANEOUS

    Brand Name : FONDAPARINUX SODIUM

    Dosage Strength : 5MG/0.4ML

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    Approval Date : 2018-11-14

    Application Number : 208615

    Regulatory Info : RX

    Registration Country : USA

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    FONDAPARINUX SODIUM

    ScinoPharm Taiwan, Ltd

    Dosage Form : INJECTABLE;SUBCUTANEOUS

    Brand Name : FONDAPARINUX SODIUM

    Dosage Strength : 7.5MG/0.6ML

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    Approval Date : 2018-11-14

    Application Number : 208615

    Regulatory Info : RX

    Registration Country : USA

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    FONDAPARINUX SODIUM

    ScinoPharm Taiwan, Ltd

    Dosage Form : INJECTABLE;SUBCUTANEOUS

    Brand Name : FONDAPARINUX SODIUM

    Dosage Strength : 10MG/0.8ML

    Packaging :

    Approval Date : 2018-11-14

    Application Number : 208615

    Regulatory Info : RX

    Registration Country : USA

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