欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3303/002
药品名称Alprostadil Recordati 3 mg/g cream
活性成分
    • alprostadil 3.0 mg/g
剂型Cream
上市许可持有人Recordati Ireland Raheens East, Ringaskiddy Co. Cork Ireland
参考成员国 - 产品名称Netherlands (NL)
Alprostadil Recordati 3 mg/g Crème
互认成员国 - 产品名称
    • Ireland (IE)
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
      VITAROS
    • Cyprus (CY)
    • Czechia (CZ)
      Vitaros 3 mg/ g krém
    • Romania (RO)
      VITAROS 3 mg/g cremă
    • Slovakia (SK)
      Vitaros 3 mg/g krém
许可日期2015/08/06
最近更新日期2023/09/05
药物ATC编码
    • G04BE01 alprostadil
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • 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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase