欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5571/001
药品名称Doxorubicin pegylated liposomal SUN 2 mg/ml concentrate for solution for infusion
活性成分
    • Doxorubicin 2.0 mg/ml
剂型Concentrate for solution for infusion
上市许可持有人Sun Pharmaceutical Industries Europe BV Polarisavenue 87 2132 JH Hoofddorp The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Doxorubicine gepegyleerd liposomaal SUN 2 mg/ml concentraat voor oplossing voor infusie
互认成员国 - 产品名称
    • Spain (ES)
    • Slovakia (SK)
    • Finland (FI)
    • Germany (DE)
      Doxorubicin pegyliert liposomal SUN 2 mg/ml Infusionslösungskonzentrat
    • France (FR)
    • Hungary (HU)
    • Ireland (IE)
    • Italy (IT)
    • Norway (NO)
    • Austria (AT)
    • Poland (PL)
    • Belgium (BE)
    • Portugal (PT)
    • Czechia (CZ)
      Doxorubicin peg-lyposomalis SUN
    • Romania (RO)
      Doxorubicină lipozomală polietilenglicată SUN 2 mg/ml concentrat pentru soluţie perfuzabilă
    • Denmark (DK)
    • Sweden (SE)
    • Greece (GR)
    • Slovenia (SI)
许可日期2023/09/13
最近更新日期2024/11/19
药物ATC编码
    • L01DB01 doxorubicin
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
    市场状态Withdrawn(注:已撤市)
    ©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase