欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3936/002
药品名称Anagrelide Housthon 1 mg, harde capsules
活性成分
    • anagrelide 1.0 mg
剂型Capsule, hard
上市许可持有人Accord Healthcare B.V. Winthontlaan 200 3526 KV Utrecht Netherlands
参考成员国 - 产品名称Netherlands (NL)
Anagrelide Housthon 1 mg, harde capsules
互认成员国 - 产品名称
    • Portugal (PT)
    • Italy (IT)
    • Poland (PL)
      Anagrelide Accord
    • Romania (RO)
许可日期2017/10/05
最近更新日期2023/06/26
药物ATC编码
    • L01XX35 anagrelide
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Other Generic application Art 10.3 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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