欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号AT/H/1220/001
药品名称Lapatinib TEVA 250 mg Filmtabletten
活性成分
    • Lapatinib 250.0 mg
剂型Film-coated tablet
上市许可持有人ratiopharm Arzneimittel Vertriebs-GmbH Donau-City-Straße 11, Ares Tower, Top 13 1220 Vienna Austria
参考成员国 - 产品名称Austria (AT)
互认成员国 - 产品名称
    • Portugal (PT)
    • Sweden (SE)
    • Hungary (HU)
      Lapatinib Teva 250 mg filmtabletta
    • Czechia (CZ)
      Lapatinib Teva
    • Slovakia (SK)
    • Croatia (HR)
    • France (FR)
许可日期2023/08/09
最近更新日期2025/01/24
药物ATC编码
    • L01EH01 lapatinib
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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