欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3946/002
药品名称Prasugrel
活性成分
    • Prasugrelhydrobromid 10.0 mg
剂型Film-coated tablet
上市许可持有人Teva B.V. Swensweg 5 2031 GA Haarlem The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Prasugrel Teva 10 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Bulgaria (BG)
      Prasugrel Teva
    • Germany (DE)
      Prasugrel-ratiopharm 10 mg Filmtabletten
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Prasugrel ratiopharm 10 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Croatia (HR)
      Prasugrel Pliva 10 mg filmom obložene tablete
许可日期2018/02/09
最近更新日期2023/07/11
药物ATC编码
    • B01AC22 prasugrel
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • 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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