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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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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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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    Polatuzumab Vedotin

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    F. Hoffmann-La Roche

    Switzerland
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    F. Hoffmann-La Roche

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    Registration Country : Switzerland

    Polatuzumabum vedotinum

    Brand Name : Polivy

    Dosage Form : Dry Sub

    Dosage Strength : 140mg

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    Registration Country : Switzerland

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    F. Hoffmann-La Roche

    Switzerland
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    F. Hoffmann-La Roche

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    Registration Country : Switzerland

    Polatuzumabum vedotinum

    Brand Name : Polivy

    Dosage Form : Trockensub

    Dosage Strength : 30mg

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    Registration Country : Switzerland

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    F. Hoffmann-La Roche

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    Regulatory Info : Prescription

    Registration Country : Canada

    POLATUZUMAB VEDOTIN

    Brand Name : POLIVY

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 30MG/VIAL

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    Approval Date :

    Application Number : 2515431

    Regulatory Info : Prescription

    Registration Country : Canada

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    F. Hoffmann-La Roche

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    POLATUZUMAB VEDOTIN

    Brand Name : POLIVY

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 140MG/VIAL

    Packaging :

    Approval Date :

    Application Number : 2499614

    Regulatory Info : Prescription

    Registration Country : Canada

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    05

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    U.S.A
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    POLATUZUMAB VEDOTIN-PIIQ

    Brand Name : POLIVY

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : 140MG/VIAL

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    Approval Date :

    Application Number : 761121

    Regulatory Info :

    Registration Country : USA

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    06

    Genentech

    U.S.A
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    Regulatory Info :

    Registration Country : USA

    POLATUZUMAB VEDOTIN-PIIQ

    Brand Name : POLIVY

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : 30MG/VIAL

    Packaging :

    Approval Date :

    Application Number : 761121

    Regulatory Info :

    Registration Country : USA

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