欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SI/H/0299/001
药品名称Apixaban Grindeks 2.5 mg film-coated tablets
活性成分
    • Apixaban 2.5 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Slovenia (SI)
Apiksaban Grindeks 2,5 mg filmsko obložene tablete
互认成员国 - 产品名称
    • Estonia (EE)
    • France (FR)
    • Hungary (HU)
    • Spain (ES)
    • Bulgaria (BG)
      Apixaban Grindeks 2.5 mg film-coated tablets
    • Portugal (PT)
    • Czechia (CZ)
      Apixaban Grindeks
    • Italy (IT)
    • Romania (RO)
      Apixaban Grindeks 2.5 mg comprimate filmate
    • Greece (GR)
    • Slovakia (SK)
    • Sweden (SE)
    • Croatia (HR)
    • Germany (DE)
      Apixaban Grindeks 2,5 mg Filmtabletten
    • Norway (NO)
    • Denmark (DK)
    • Finland (FI)
    • Belgium (BE)
    • Poland (PL)
      Apixaban Grindeks
    • Netherlands (NL)
      Apixaban Grindeks 2,5 mg, filmomhulde tabletten
    • Latvia (LV)
    • Ireland (IE)
    • Lithuania (LT)
      Apixaban Grindeks 2,5 mg plėvele dengtos tabletės
    • Austria (AT)
许可日期2025/07/14
最近更新日期2025/08/13
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
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市场状态Positive
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