欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HR/H/0185/001
药品名称Sugammadex Teva 100 mg/ml solution for injection
活性成分
    • Sugammadex sodium 100.0 mg/ml
剂型Solution for injection
上市许可持有人Teva B.V. Swensweg 5 2031GA Haarlem Netherlands
参考成员国 - 产品名称Croatia (HR)
互认成员国 - 产品名称
    • Netherlands (NL)
    • Slovenia (SI)
    • Ireland (IE)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Germany (DE)
      Sugammadex-ratiopharm 100 mg/ml Injektionslösung
    • Poland (PL)
    • Denmark (DK)
    • Hungary (HU)
    • Romania (RO)
      Sugammadex TEVA 100 mg/ml solution for injection
许可日期2022/01/10
最近更新日期2024/10/24
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
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase