欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5766/002
药品名称Enzalutamide Teva 80 mg, Film-coated tablet
活性成分
    • enzalutamide 80.0 mg
剂型Film-coated tablet
上市许可持有人Teva Nederland B.V. Swensweg 5 2031 GA Haarlem The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Enzalutamide Teva 80 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Spain (ES)
    • Slovenia (SI)
    • Portugal (PT)
    • Croatia (HR)
    • Italy (IT)
    • Greece (EL)
    • Germany (DE)
      Enzalutamid-ratiopharm 80 mg Filmtabletten
    • Sweden (SE)
    • Denmark (DK)
      Enzalutamide Teva
    • Norway (NO)
    • Belgium (BE)
    • Finland (FI)
    • Luxembourg (LU)
    • Hungary (HU)
    • Iceland (IS)
    • Bulgaria (BG)
      Enzalutamide Teva 80 mg film-coated tablet
    • Ireland (IE)
    • Cyprus (CY)
      Enzalutamide/Teva 80 mg film-coated tablets
    • Austria (AT)
    • Czech Republic (CZ)
      Enzalutamid Teva
    • France (FR)
    • Romania (RO)
许可日期2025/10/23
最近更新日期2025/10/23
药物ATC编码
    • L02BB04 enzalutamide
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Generic
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
附件文件下载
    市场状态Positive
    ©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase