欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4962/002
药品名称Abiraterone 500 mg
活性成分
    • Abiraterone acetate 500.0 mg
剂型Film-coated tablet
上市许可持有人Synthon BV, Netherlands
参考成员国 - 产品名称Netherlands (NL)
Abiraterone Synthon 500 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
      Abirateron Synthon 500 mg Tabletten
    • Bulgaria (BG)
      Abiraterone Haeton
    • Iceland (IS)
    • Malta (MT)
    • Spain (ES)
    • Greece (GR)
    • Sweden (SE)
      Abirateron Avansor
    • Finland (FI)
    • Poland (PL)
      Abiraterone Synthon
    • Czechia (CZ)
      Abiraterone acetate Heaton 500 mg
    • Slovakia (SK)
    • Croatia (HR)
      Abirateron Alpha-Medical 500 mg filmom obložene tablete
许可日期2021/03/10
最近更新日期2024/10/15
药物ATC编码
    • L02BX03 abiraterone
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • 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
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