欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/7512/001
药品名称Sugammadex Baxter 100 mg/ml Injektionslösung
活性成分
    • Sugammadex sodium 100.0 mg/ml
剂型Solution for injection
上市许可持有人Baxter Holding B.V. Kobaltweg 49 3542 CE Utrecht Netherlands
参考成员国 - 产品名称Germany (DE)
Sugammadex Baxter 100 mg/ml Injektionslösung
互认成员国 - 产品名称
    • Romania (RO)
      Sugammadex Baxter 100 mg/ml soluție injectabilă
    • Austria (AT)
    • Slovenia (SI)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Denmark (DK)
      Sugammadex "Baxter"
    • Finland (FI)
    • Belgium (BE)
      Sugammadex Baxter 100 mg/ml solution injectable
    • Poland (PL)
    • Netherlands (NL)
    • Czechia (CZ)
      Sugammadex Baxter
    • Ireland (IE)
许可日期2023/06/16
最近更新日期2024/03/14
药物ATC编码
    • V03AB35 sugammadex
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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