欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/6093/002
药品名称Ticagrelor AL 90 mg Filmtabletten
活性成分
    • Ticagrelor 90.0 mg
剂型Film-coated tablet
上市许可持有人ALIUD PHARMA GmbH Gottlieb-Daimler-Str. 19 89150 Laichingen Germany
参考成员国 - 产品名称Germany (DE)
Ticagrelor AL 90 mg Filmtabletten
互认成员国 - 产品名称
    • Sweden (SE)
    • Finland (FI)
    • Denmark (DK)
    • Czechia (CZ)
      Ticagrelor STADA
    • Belgium (BE)
      Ticagrelor EG 90 mg filmomhulde tabletten
    • Romania (RO)
    • Netherlands (NL)
    • Slovakia (SK)
      Tikagrelor STADA 90 mg filmom obalené tablety
    • Luxembourg (LU)
    • Slovenia (SI)
    • Iceland (IS)
    • Austria (AT)
      Ticagrelor STADA 90 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
许可日期2021/06/02
最近更新日期2024/11/14
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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