欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DK/H/3216/001
药品名称Abirateron Teva
活性成分
    • abiraterone acetate 500.0 mg
剂型Film-coated tablet
上市许可持有人Teva B.V. Swensweg 5 2031GA Haarlem, Netherlands
参考成员国 - 产品名称Denmark (DK)
Abirateron "Teva"
互认成员国 - 产品名称
    • Latvia (LV)
    • Ireland (IE)
    • Lithuania (LT)
    • Austria (AT)
    • Estonia (EE)
    • France (FR)
    • Hungary (HU)
      Abirateron Teva 500 mg filmtabletta
    • Spain (ES)
    • Bulgaria (BG)
      Abiraterone Teva
    • Portugal (PT)
    • Czechia (CZ)
      Abirateron Teva
    • Italy (IT)
    • Romania (RO)
    • Greece (GR)
    • Slovenia (SI)
    • Sweden (SE)
    • Croatia (HR)
    • Germany (DE)
      Abirateronacetat-ratiopharm 500 mg Filmtabletten
    • Norway (NO)
    • Finland (FI)
    • Netherlands (NL)
    • Poland (PL)
    • Iceland (IS)
许可日期2022/05/04
最近更新日期2023/12/01
药物ATC编码
    • L02BX03 abiraterone
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • 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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