欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5597/002
药品名称Sugammadex Aguettant 50 mg/ml solution for injection in prefilled syringe
活性成分
    • Sugammadex sodium 50.0 mg/ml
剂型Solution for injection in pre-filled syringe
上市许可持有人Laboratoire Aguettant 1 Rue Alexander Fleming 69007 Lyon France
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Germany (DE)
    • Poland (PL)
      Sugammadex Aguettant
    • Denmark (DK)
      Sugammadex Aguettant
    • Hungary (HU)
    • Belgium (BE)
    • Romania (RO)
      Sugammadex Aguettant 50 mg/mL solutie injectabilă în seringă preumplută
    • Ireland (IE)
许可日期2023/08/02
最近更新日期2025/01/29
药物ATC编码
    • V03AB35 sugammadex
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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