欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号HR/H/0189/002
药品名称Apixaban Krka 5 mg film-coated tablets
活性成分
    • APIXABAN 5.0 mg
剂型Film-coated tablet
上市许可持有人Krka d.d. Novo Mesto, Smarjeska Cesta 6, 8501 Novo Mesto, Slovenia
参考成员国 - 产品名称Croatia (HR)
Apiksaban Krka 5 mg filmom obložene tablete
互认成员国 - 产品名称
    • Norway (NO)
    • Denmark (DK)
    • Finland (FI)
    • Belgium (BE)
      Apixaban Krka 5 mg filmomhulde tabletten
    • United Kingdom (Northern Ireland) (XI)
    • Netherlands (NL)
      Apixaban HCS 5 mg filmomhulde tabletten
    • Iceland (IS)
      Apixaban Krka
    • Ireland (IE)
    • Austria (AT)
      Apixaban HCS 5 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
许可日期2021/09/17
最近更新日期2022/06/02
药物ATC编码
    • B01AF02 apixaban
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
附件文件下载
市场状态Positive
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