欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/2087/001
药品名称Clarithromycin 250 mg
活性成分
    • clarithromycin 250.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Belgium (BE)
    • Spain (ES)
    • Poland (PL)
    • Bulgaria (BG)
      Clarithromycin Sandoz
    • Romania (RO)
      Claritromicina Sandoz 250 mg comprimate filmate
    • Slovakia (SK)
      LEKOKLAR 250 mg filmom obalené tablety
许可日期2011/08/29
最近更新日期2024/03/04
药物ATC编码
    • J01FA09 clarithromycin
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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