欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4152/001
药品名称Gefitinib 250 mg Film-coated Tablets
活性成分
    • gefitinib 250.0 mg
剂型Film-coated tablet
上市许可持有人Teva B.V. Swensweg 5 2031GA Haarlem
参考成员国 - 产品名称Netherlands (NL)
Gefitinib Teva 250 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
      Gefitinib-ratiopharm 250 mg Filmtabletten
    • Belgium (BE)
      Gefitinib Teva 250 mg filmomhulde tabletten
    • Luxembourg (LU)
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Lithuania (LT)
      Gefitinib Teva 250 mg plėvele dengtos tabletės
    • Hungary (HU)
      GEFITINIB TEVA 250 mg filmtabletta
    • Bulgaria (BG)
      Gefitinib Teva
    • Croatia (HR)
      Gefitinib Pliva 250 mg filmom obložene tablete
许可日期2018/10/05
最近更新日期2024/08/14
药物ATC编码
    • L01XE02 gefitinib
申请类型
  • TypeLevel1:Known Active Substance
  • 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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