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

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    pharmacompass-1-m-2026-01-12

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    End-to-end drug development, specializing in high-potency softgels and liquids, providing global partners with a competitive advantage.

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    Kewpie is your partner for Sodium Hyaluronate & Hyaluronic Acid// CEP, USDMF, KDMF & JDMF registered.

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    Durvalumab

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    Astrazeneca Ab

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    Regulatory Info : Approved

    Registration Country : Sweden

    Durvalumab

    Brand Name : Imfinzi

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength : 50mg/ml

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    Approval Date : 21/09/2018

    Application Number : 20170905000017

    Regulatory Info : Approved

    Registration Country : Sweden

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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Durvalumabum

    Brand Name : Imfinzi

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength : 120mg/2.4ml

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    Approval Date : 11/06/2018

    Application Number : 66548

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Durvalumabum

    Brand Name : Imfinzi

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength : 500mg/10ml

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    Approval Date : 11/06/2018

    Application Number : 66548

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    Regulatory Info : Authorized

    Registration Country : Spain

    Durvalumab

    Brand Name : Imfinzi

    Dosage Form : Concentrate For Infusion Solution

    Dosage Strength : 50MG

    Packaging :

    Approval Date : 2020-11-03

    Application Number : 1181322001IP

    Regulatory Info : Authorized

    Registration Country : Spain

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    Regulatory Info : Authorized

    Registration Country : Spain

    Durvalumab

    Brand Name : Imfinzi

    Dosage Form : Concentrate For Infusion Solution

    Dosage Strength : 50MG

    Packaging :

    Approval Date : 2020-11-03

    Application Number : 1181322002IP

    Regulatory Info : Authorized

    Registration Country : Spain

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    06

    Astrazeneca Ab

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    Regulatory Info : Authorized

    Registration Country : Spain

    Durvalumab

    Brand Name : Imfinzi

    Dosage Form : Concentrate For Infusion Solution

    Dosage Strength : 50MG

    Packaging :

    Approval Date : 2018-10-31

    Application Number : 1181322002

    Regulatory Info : Authorized

    Registration Country : Spain

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    07

    Astrazeneca Ab

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    Regulatory Info : Authorized

    Registration Country : Spain

    Durvalumab

    Brand Name : Imfinzi

    Dosage Form : Concentrate For Infusion Solution

    Dosage Strength : 50MG

    Packaging :

    Approval Date : 2018-10-31

    Application Number : 1181322001

    Regulatory Info : Authorized

    Registration Country : Spain

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    08

    Astrazeneca Ab

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    Astrazeneca Ab

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    Regulatory Info :

    Registration Country : Moldova

    Durvalumab

    Brand Name : Imfinzi 50 mg/ml

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength : 120mg/2.4ml

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    Approval Date : 27-05-2022

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    Regulatory Info :

    Registration Country : Moldova

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    09

    Astrazeneca Ab

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    Astrazeneca Ab

    United Kingdom
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    VMX
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    • fda
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info :

    Registration Country : Moldova

    Durvalumab

    Brand Name : Imfinzi 50 mg/ml

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength :

    Packaging :

    Approval Date : 27-05-2022

    Application Number :

    Regulatory Info :

    Registration Country : Moldova

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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.