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

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    Erdafitinib

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    Regulatory Info : RX

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    ERDAFITINIB

    Brand Name : BALVERSA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 3MG

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    Approval Date : 2019-04-12

    Application Number : 212018

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : BALVERSA

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    ERDAFITINIB

    Brand Name : BALVERSA

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    Application Number : 2493217

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    Erdafitinib

    Brand Name : Balversa

    Dosage Form : Film Coated Tablet

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    Approval Date : 14/01/2025

    Application Number : 67660

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    Brand Name : Balversa

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    Approval Date : 14/01/2025

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    Erdafitinib

    Brand Name : Balversa

    Dosage Form : Film Coated Tablet

    Dosage Strength : 5mg

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    Approval Date : 14/01/2025

    Application Number : 67660

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    10

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    Regulatory Info : Marketed

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    Brand Name : Balversa

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    Registration Country : Estonia

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    Erdafitinib

    Brand Name : Balversa

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    Approval Date : 27-08-2024

    Application Number : 1241841004

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    Brand Name : Balversa

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    Approval Date : 27-08-2024

    Application Number : 1241841009

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    Approval Date : 27-08-2024

    Application Number : 1241841011

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    Erdafitinib

    Brand Name : Balversa

    Dosage Form : Film Coated Tablet

    Dosage Strength : 3mg

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    Approval Date : 22-08-2024

    Application Number : 28107045223

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    Registration Country : Denmark

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    Approval Date : 22-08-2024

    Application Number : 28107045423

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