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Mundipharma Corporation (Ireland) LimitedEU/1/17/1238/001

Main Information

Trade NameNyxoid
Active SubstancesNaloxone hydrochloride dihydrate
Dosage FormNasal spray, solution in single-dose container
Licence HolderMundipharma Corporation (Ireland) Limited
Licence NumberEU/1/17/1238/001

Group Information

ATC CodeV03AB Antidotes
V03AB15 naloxone


License statusAuthorised
Licence Issued10/11/2017
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of Licence
Marketing StatusUnknown


Summary of Product CharacteristicsSearch EMA website
Package LeafletSearch EMA website
Public Assessment ReportSearch EMA website
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