欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/5343/001
药品名称Gefitinib Accord 250 mg Filmtabletten
活性成分
    • gefitinib 250.0 mg
剂型Film-coated tablet
上市许可持有人Accord Healthcare B.V. Winthontlaan 200 NL-3526 KV Utrecht Netherlands
参考成员国 - 产品名称Germany (DE)
Gefitinib 250 mg Filmtabletten
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Gefitinib Accord 250 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Finland (FI)
    • Poland (PL)
      Gefitinib Accord
    • Czechia (CZ)
      Gefitinib Accord 250 mg potahované tablety
    • Romania (RO)
      Gefitinib Accord 250 mg comprimate filmate
    • Denmark (DK)
    • Belgium (BE)
      Gefitinib Accord 250 mg Filmomhulde tabletten
许可日期2018/12/05
最近更新日期2024/04/09
药物ATC编码
    • L01XE02 gefitinib
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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