欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HU/H/0662/001
药品名称Atixarso 60 mg film-coated tablet
活性成分
    • Ticagrelor 60.0 mg
剂型Film-coated tablet
上市许可持有人Krka d.d. Novo Mesto Smarjeska Cesta 6 Novo Mesto 8501 Slovenia Telephone +386 7 331 21 11 E-mail regulatory.affairs@krka.biz
参考成员国 - 产品名称Hungary (HU)
互认成员国 - 产品名称
    • Estonia (EE)
      ATIXARSO
    • Bulgaria (BG)
      Tilyrol
    • Czechia (CZ)
      Tilyrol
    • Romania (RO)
      Tilyrol 60 mg comprimate filmate
    • Slovakia (SK)
      Atixarso 60 mg filmom obalené tablety
    • Slovenia (SI)
      Atixarso 60 mg filmsko obložene tablete
    • Croatia (HR)
      Atixarso 60 mg filmom obložene tablete
    • Greece (GR)
    • Poland (PL)
    • Latvia (LV)
      Atixarso 60 mg apvalkotās tabletes
    • Lithuania (LT)
      Atixarso 60 mg plėvele dengtos tabletės
许可日期2020/11/30
最近更新日期2024/06/12
药物ATC编码
    • B01AC24 ticagrelor
申请类型
  • TypeLevel1：Known Active Substance
  • 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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