欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号IS/H/0494/003
药品名称Rivaroxaban Grindeks
活性成分
    • Rivaroxaban 20.0 mg
剂型Film-coated tablet
上市许可持有人Grindeks AS Krustpils Iela 53 1057 Riga Latvia
参考成员国 - 产品名称Iceland (IS)
Rivaroxaban Grindeks
互认成员国 - 产品名称
    • Romania (RO)
      Rivaroxaban Grindeks 20 mg comprimate filmate
    • Greece (GR)
    • Slovakia (SK)
    • Germany (DE)
    • Sweden (SE)
    • Slovenia (SI)
    • Denmark (DK)
    • Norway (NO)
    • Croatia (HR)
    • Belgium (BE)
      Rivaroxaban Grindeks 20 mg filmomhulde tabletten
    • Finland (FI)
    • Netherlands (NL)
    • Poland (PL)
    • Luxembourg (LU)
    • Latvia (LV)
    • Ireland (IE)
    • Lithuania (LT)
      Rivaroxaban Grindeks 20 mg plėvele dengtos tabletės
    • Austria (AT)
    • Estonia (EE)
    • France (FR)
    • Hungary (HU)
    • Spain (ES)
    • Bulgaria (BG)
    • Portugal (PT)
    • Czechia (CZ)
      Rivaroxaban Grindeks
    • Italy (IT)
许可日期2025/05/05
最近更新日期2025/07/24
药物ATC编码
    • B01AF01 rivaroxaban
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
附件文件下载
市场状态Positive
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