欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4790/001
药品名称Lerdip 10 mg, filmomhulde tabletten
活性成分
    • Lercanidipine Hydrochloride 10.0 mg
剂型Film-coated tablet
上市许可持有人Recordati Ireland Ltd. (Co. Cork) Raheens East P43 KD30 Ringaskiddy, Cork Ireland
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Germany (DE)
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
    • Austria (AT)
      Zanidip 10 mg Filmtabletten
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Finland (FI)
许可日期2008/04/05
最近更新日期2024/04/18
药物ATC编码
    • A ALIMENTARY TRACT AND METABOLISM
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase