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Mundipharma announces EU regulatory submission for Nyxoid

Mundipharma have submitted a marketing authorisation application for Nyxoid (intranasal naloxone 1.8 mg in 0.1 ml) to the European Medicines Agency (EMA), seeking approval for the emergency reversal of opioid overdose.


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source: http://www.europeanpharmaceuticalreview.com/45212/news/industry-news/mundipharma-opioid-overdose/

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