欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号CZ/H/0723/001
药品名称LOPERAMID DR.MAX 2 mg capsule hard
活性成分
    • Loperamide hydrochloride 2.0 mg
剂型Capsule, hard
上市许可持有人Dr. Max Pharma s.r.o. Na Florenci 2116/15 110 00 Praha 1 - Nové Město
参考成员国 - 产品名称Czechia (CZ)
LOPERAMID DR.MAX
互认成员国 - 产品名称
    • Romania (RO)
      Loperamid Dr.Max 2 mg capsule
    • Poland (PL)
    • Slovakia (SK)
      Loperamid Farmax 2 mg
许可日期2017/10/26
最近更新日期2024/11/13
药物ATC编码
    • A07DA03 loperamide
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:Non Prescription (including OTC)
附件文件下载
市场状态Positive
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase