欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5765/001
药品名称Rivaroxaban Sandoz twice daily 10 mg, film-coated tablets
活性成分
    • RIVAROXABAN 10.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Rivaroxaban Sandoz 2xdaags 10mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
许可日期2024/05/16
最近更新日期2024/05/17
药物ATC编码
    • B01AF01 rivaroxaban
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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    市场状态Withdrawn(注:已撤市)
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