欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/4815/001
药品名称Ticagrelor Viatris 60 mg, filmomhulde tabletten
活性成分
    • Ticagrelor 60.0 mg
剂型Film-coated tablet
上市许可持有人Viatris Ltd Damastown Industrial Park Mulhuddart Dublin 15 Dublin Ierland
参考成员国 - 产品名称Netherlands (NL)
Ticagrelor Viatris 60 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Ireland (IE)
    • Sweden (SE)
    • Austria (AT)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Germany (DE)
      Ticagrelor Mylan 60 mg Filmtabletten
    • Norway (NO)
    • Denmark (DK)
    • Finland (FI)
    • Cyprus (CY)
      Ticagrelor Pharos 60mg, FCT
    • Czechia (CZ)
      Ticagrelor PharOs
    • United Kingdom (Northern Ireland) (XI)
    • Iceland (IS)
      Ticagrelor
许可日期2020/11/20
最近更新日期2025/08/28
药物ATC编码
    • B01AC24 ticagrelor
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
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市场状态Positive
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