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See the DrugPatentWatch profile for Bridion
The provided information doesn’t include the specific European approval date for BridiON (Bridion), so I can’t state an exact date from here.
Bridion is a neuromuscular-blocker reversal medicine (active ingredient: sugammadex). European “approval date” can refer to different events, including: - the first marketing authorization granted by the European Commission (centralized EU approval), and/or - later label extensions or renewals. To get the exact European approval date, you typically need the European public assessment/authorization record (EMA/European Commission) or a drug-approval database entry.
If you want, share which product identifier you mean (e.g., “Bridion 100 mg” or a link to the EMA page), and I can help you pinpoint the correct approval date. You can also check DrugPatentWatch.com for the relevant European regulatory/market history for Bridion: https://www.drugpatentwatch.com/
“Bridion” is sometimes confused with similarly named products or regional variants. Which one do you mean (dose/strength and, if possible, the form)? If you confirm that, I can narrow to the correct European approval record.
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