欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号EE/H/0125/001
药品名称Azimepha 250 mg
活性成分
    • azithromycin 250.0 mg
剂型Film-coated tablet
上市许可持有人Ex: FI/H/682/01 Mepha Investigação, Desenvolvimento e Fabricação Famacêutica, Lda. Lagoas Park Edifício 5 A, Piso 2 2740-298 Porto Salvo Portugal RMS transfer from FI to EE. Old procedure number: FI/H/682/01
参考成员国 - 产品名称Estonia (EE)
互认成员国 - 产品名称
    • Latvia (LV)
    • Lithuania (LT)
      Azimepha 250 mg plėvele dengtos tabletės
    • Malta (MT)
许可日期2009/05/04
最近更新日期2013/01/14
药物ATC编码
    • J01FA10 azithromycin
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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