欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4322/001
药品名称Tadalafil AOP
活性成分
    • Tadalafil 20.0 mg
剂型Film-coated tablet
上市许可持有人Aop Orphan Pharmaceuticals GmbH Leopold-Ungar-Platz 2 1190 Vienna Austria
参考成员国 - 产品名称Netherlands (NL)
Tadalafil AOP 20 mg filmomhulde tabletten
互认成员国 - 产品名称
    • Austria (AT)
      Tadalafil AOP 20 mg Filmtabletten
    • Sweden (SE)
    • Finland (FI)
    • Latvia (LV)
      Tadalafil AOP 20 mg apvalkotās tabletes
    • Lithuania (LT)
      Tadalafil AOP 20 mg plėvele dengtos tabletės
    • Hungary (HU)
      TADALAFIL AOP 20 mg filmtabletta
    • Czechia (CZ)
      Tadalafil AOP 20 mg potahované tablety
    • Slovakia (SK)
      Tadalafil AOP 20 mg filmom obalené tablety
    • Slovenia (SI)
      Tadalafil AOP Orphan 20 mg filmsko obložene tablete
    • Croatia (HR)
      Tadalafil AOP 20 mg filmom obložene tablete
许可日期2019/01/29
最近更新日期2025/01/09
药物ATC编码
    • G04BE08 tadalafil
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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