欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5278/002
药品名称Abirate 1A Pharma 500 mg, filmomhulde tabletten
活性成分
    • abiraterone acetate 500.0 mg
剂型Film-coated tablet
上市许可持有人1 A Pharma GmbH Keltenring 1+3 Oberhaching 82041 Bavaria Germany
参考成员国 - 产品名称Netherlands (NL)
Abirate 1A Pharma 500 mg, filmomhulde
互认成员国 - 产品名称
    • Germany (DE)
      Abirate HEXAL 500 mg Filmtabletten
许可日期2021/04/20
最近更新日期2021/04/21
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Withdrawn(注:已撤市)
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