欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5716/002
药品名称Ticagrelor Xiromed 90 mg, Film-coated tablets
活性成分
    • Ticagrelor 90.0 mg
剂型Film-coated tablet
上市许可持有人Medical Valley Invest AB Bradgardsvagen 28 2 Tr 236 32 Hollviken Skane Lan Sweden
参考成员国 - 产品名称Netherlands (NL)
Ticagrelor Xiromed 90 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Sweden (SE)
    • Norway (NO)
    • Poland (PL)
      Ticagrelor Medical Valley
    • Germany (DE)
      Ticagrelor AXiromed 90 mg Filmtabletten
    • Denmark (DK)
      Ticagrelor "Medical Valley"
    • Iceland (IS)
许可日期2024/02/07
最近更新日期2025/02/05
药物ATC编码
    • B01AC24 ticagrelor
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • 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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