欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4790/002
药品名称Lerdip 20 mg, filmomhulde tabletten
活性成分
    • Lercanidipine hydrochloride 20.0 mg
剂型Film-coated tablet
上市许可持有人Recordati Industria Chimica & Farmaceutica S.P.A Via M. Civitali 1-20148 Milano ITALY
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)
    • Austria (AT)
      Zanidip 20 mg-Filmtabletten
    • Spain (ES)
      Zanidip 20 mg comprimidos recubiertos con película
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
      Zanidip
    • Finland (FI)
许可日期2008/04/05
最近更新日期2024/12/18
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
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