欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/7374/002
药品名称Ticagrelor AbZ 90 mg Filmtabletten
活性成分
    • Ticagrelor 90.0 mg
剂型Film-coated tablet
上市许可持有人Teva B.V. Swensweg 5 2031GA Haarlem Netherlands
参考成员国 - 产品名称Germany (DE)
Ticagrelor AbZ 90 mg Filmtabletten
互认成员国 - 产品名称
    • Finland (FI)
      Ticagrelor ratiopharm
    • Latvia (LV)
    • Denmark (DK)
      Ticagrelor Teva
    • Lithuania (LT)
      Ticagrelor Teva 90 mg plėvele dengtos tabletės
    • Belgium (BE)
    • Estonia (EE)
    • Netherlands (NL)
    • Czechia (CZ)
      Ticagrelor Teva
    • Ireland (IE)
    • Slovakia (SK)
    • Austria (AT)
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
许可日期2023/11/23
最近更新日期2024/05/21
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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市场状态Positive
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