欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/3953/001
药品名称Fulvestrant SUN 250 mg solution for injection in prefilled syringe
活性成分
    • fulvestrant 250.0 mg
剂型Solution for injection
上市许可持有人Sun Pharmaceutical Industries Europe B.V. Polarisavenue 87 2132 JH HOOFDDORP The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Fulvestrant Sun 250 mg oplossing voor injectie in voorgevulde spuit
互认成员国 - 产品名称
    • Denmark (DK)
    • Norway (NO)
    • Germany (DE)
      Fulvestrant SUN 250 mg Injektionslösung in einer Fertigspritze
    • United Kingdom (Northern Ireland) (XI)
    • Spain (ES)
    • Italy (IT)
    • Sweden (SE)
    • Poland (PL)
      Fulvestrant SUN
    • Romania (RO)
许可日期2018/03/29
最近更新日期2024/03/06
药物ATC编码
    • L02BA03 fulvestrant
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
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市场状态Positive
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