欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HU/H/0812/001
药品名称Sugammadex Gebro
活性成分
    • Sugammadex sodium 100.0 mg/ml
剂型Solution for injection
上市许可持有人Gebro Pharma GmbH 6391 Fieberbrunn Austria
参考成员国 - 产品名称Hungary (HU)
Sugammadex Gebro 100 mg/ml solution for injection
互认成员国 - 产品名称
    • Netherlands (NL)
    • Luxembourg (LU)
    • Austria (AT)
    • Spain (ES)
    • Portugal (PT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Germany (DE)
      Sugammadex Gebro 100 mg/ml Injektionslösung
    • Belgium (BE)
      Sugammadex Gebro 100 mg/ml solution injectable
许可日期2022/11/22
最近更新日期2024/11/06
药物ATC编码
    • V03AB35 sugammadex
申请类型
  • TypeLevel1：Known Active Substance
  • 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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