欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5327/002
药品名称Rivaroxaban Sandoz
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 Nederland
参考成员国 - 产品名称Netherlands (NL)
Rivaroxaban Sandoz 10 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Sweden (SE)
      Rivaroxaban Hexal
    • Norway (NO)
    • Finland (FI)
    • Portugal (PT)
    • Hungary (HU)
      Rivaroxaban 1 A Pharma 10 mg filmtabletta
    • Czechia (CZ)
      Rivaroxaban Sandoz
    • Germany (DE)
      Rivaroxaban HEXAL 10 mg Filmtabletten
    • Denmark (DK)
      Rivaroxaban "Hexal"
    • Iceland (IS)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
许可日期2022/03/22
最近更新日期2025/01/29
药物ATC编码
    • B01AF01 rivaroxaban
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
附件文件下载
市场状态Positive
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