欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/3612/002
药品名称Tadalafil Sandoz 5 mg film-coated tablets
活性成分
    • Tadalafil 5.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz BV Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Tadalafil Sandoz 5 mg filmomhulde tabletten
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
      Tadalafil Sandoz 5 mg film-coated tablets
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Tadalafil Sandoz 5 mg – Filmtabletten
    • Portugal (PT)
    • Sweden (SE)
    • Norway (NO)
      Tadalafil Sandoz
    • Finland (FI)
    • Slovenia (SI)
      Tadalafil Lek 5 mg filmsko obložene tablete
许可日期2016/11/10
最近更新日期2025/01/20
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
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase