欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号HU/H/0806/001
药品名称Loperamide Grindeks 2 mg hard capsules
活性成分
    • loperamide hydrochloride 2.0 mg
剂型Capsule, hard
上市许可持有人Grindeks AS Krustpils Iela 53 1057 Riga Latvia
参考成员国 - 产品名称Hungary (HU)
互认成员国 - 产品名称
    • Sweden (SE)
    • Finland (FI)
    • Germany (DE)
      Loperamid Baltijos Bite 2 mg Hartkapseln
    • Poland (PL)
      Loperamide Grindeks
    • Belgium (BE)
      Loperamide Grindeks 2 mg harde capsules
    • Bulgaria (BG)
      Loperamide Baltijos Bite
    • Netherlands (NL)
    • Czechia (CZ)
      Loperamid Baltijos Bite
    • Ireland (IE)
    • Romania (RO)
      Loperamidă Baltijos Bite 2 mg capsule
    • Austria (AT)
    • Slovakia (SK)
    • France (FR)
    • Croatia (HR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
许可日期2023/04/25
最近更新日期2024/02/12
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
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