欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5030/001
药品名称Sugammadex Sun 100 mg/mL
活性成分
    • SUGAMMADEX sodium salt 100.0 mg/ml
剂型Solution for injection
上市许可持有人Sun Pharmaceuticals Polarisavenue 87 2132 JH Hoofddorp The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Sugammadex Sun 100 mg/ml oplossing voor injectie
互认成员国 - 产品名称
    • Germany (DE)
      Sugammadex Sun 100 mg/ml Injektionslösung
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Poland (PL)
      Sugammadex Ranbaxy
    • Romania (RO)
      Sugammadex Terapia 100 mg/ml soluţie injectabilă
许可日期2020/10/22
最近更新日期2023/10/10
药物ATC编码
    • V03AB35 sugammadex
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Multiple (Copy) 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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