欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5118/001
药品名称Sugammadex Sandoz 100 mg/ml
活性成分
    • Sugammadex sodium 100.0 mg/ml
剂型Solution for injection
上市许可持有人Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Denmark (DK)
      Sugammadex Sandoz
    • Greece (GR)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
    • Czechia (CZ)
      Sugammadex Sandoz
    • Germany (DE)
      Sugammadex HEXAL 100 mg/ml Injektionslösung
    • Romania (RO)
      Sugammadex Sandoz 100 mg/ml solutie injectabilă
    • Belgium (BE)
      Sugammadex Sandoz 100 mg/ml oplossing voor injectie
    • Slovenia (SI)
    • United Kingdom (Northern Ireland) (XI)
    • Croatia (HR)
      Sugamadeks Sandoz 100 mg/ml otopina za injekciju
    • Austria (AT)
      Sugammadex Sandoz 100 mg/ml - Injektionslösung
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
许可日期2021/02/25
最近更新日期2024/10/14
药物ATC编码
    • V03AB35 sugammadex
申请类型
  • TypeLevel1：Abridged
  • 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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