欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号AT/H/1145/001
药品名称Dexmedetomidine Hikma 100 micrograms/ml concentrate for solution for infusion
活性成分
    • Dexmedetomidine hydrochloride 100.0 µg/ml
剂型Concentrate for solution for infusion
上市许可持有人Hikma Farmacêutica (Portugal), S.A. Estrada do Rio da Mó, 8, 8A-B, Fervença 2705-906 Terrugem SNT Portugal
参考成员国 - 产品名称Austria (AT)
互认成员国 - 产品名称
    • Germany (DE)
      Dexmedetomidine Hikma
    • Netherlands (NL)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • United Kingdom (Northern Ireland) (XI)
许可日期2023/12/11
最近更新日期2025/01/18
药物ATC编码
    • N05CM18 dexmedetomidine
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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