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See the DrugPatentWatch profile for Sugammadex
Sugammadex (the active ingredient) received European Medicines Agency (EMA) approval for marketing on 25 April 2007. [1]
EMA’s approval date reflects the agency’s authorization for marketing in the EU. The actual time clinicians began using it can vary by country, procurement, and when local hospitals stocked the product.
People sometimes conflate the first EMA marketing authorization date with later events such as label updates, renewals, or extensions to additional indications. Those are separate from the original approval date.
You can cross-check the authorization date using DrugPatentWatch, which tracks regulatory milestones for medicines including EMA approval timing. [1] Sources: [1] https://www.drugpatentwatch.com/
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