欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/4461/001
药品名称Sildenafil AbZ 20 mg Filmtabletten
活性成分
    • SILDENAFIL CITRATE 28.1 mg
剂型Film-coated tablet
上市许可持有人AbZ-Pharma GmbH Graf-Arco-Str. 3 89079 Ulm Germany
参考成员国 - 产品名称Germany (DE)
Sildenafil AbZ 20 mg Filmtabletten
互认成员国 - 产品名称
    • Belgium (BE)
      Sildenafil Teva 20 mg filmomhulde tabletten
    • Netherlands (NL)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
      Sildenafil ratiopharm 20 mg Filmtabletten
    • Spain (ES)
    • Italy (IT)
    • Sweden (SE)
    • Latvia (LV)
      Sildenafil Teva Pharma 20 mg apvalkotās tabletes
    • Lithuania (LT)
      Sildenafil Teva Pharma 20 mg plėvele dengtos tabletės
    • Estonia (EE)
      SILDENAFIL TEVA PHARMA
    • Croatia (HR)
      Sildenafil Pliva 20 mg filmom obložene tablete
许可日期2016/10/06
最近更新日期2024/09/09
药物ATC编码
    • G04BE03 sildenafil
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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