欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5219/001
药品名称Abiraterone 250 Film-coated tablets
活性成分
    • abiraterone acetate 250.0 mg
剂型Film-coated tablet
上市许可持有人Centrafarm B.V. Van de Reijstraat 31 E 4814 NE Breda Netherlands Netherlands
参考成员国 - 产品名称Netherlands (NL)
Abirateron CF 250 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Belgium (BE)
      Abirateron EG 250 mg filmomhulde tabletten
    • Luxembourg (LU)
    • Italy (IT)
    • Poland (PL)
      Abiraterone STADA
    • Czechia (CZ)
      Abirateron STADA
    • Romania (RO)
      Abiraterone STADA 250 mg comprimate filmate
    • Slovakia (SK)
      Abiraterón STADA 250 mg filmom obalené tablety
许可日期2021/04/21
最近更新日期2023/12/08
药物ATC编码
    • L02BX03 abiraterone
申请类型
  • TypeLevel1:Abridged
  • 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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