欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号HU/H/0751/002
药品名称Ticagrelor Vivanta 90 mg filmtabletta
活性成分
    • Ticagrelor 90.0 mg
剂型Film-coated tablet
上市许可持有人Vivanta Generics s.r.o. Address Trtinova 260/1 Cakovice Prague 196 00 Czechia Telephone +34677433428 E-mail regulatory@vivantagenerics.com
参考成员国 - 产品名称Hungary (HU)
互认成员国 - 产品名称
    • Spain (ES)
    • Portugal (PT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Cyprus (CY)
      Ticagrelor MSN 90 mg, film-coated tablets
    • Germany (DE)
      Ticagrelor Vivanta 90 mg Filmtabletten
    • Denmark (DK)
      Ticagrelor Vivanta
    • Netherlands (NL)
      Ticagrelor Vivanta 90 mg filmomhulde tabletten
许可日期2024/02/26
最近更新日期2024/08/21
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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