欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号IE/H/0928/001
药品名称Salmeterol/Fluticasone APC 50 microgram / 500 microgram / dose inhalation powder, pre-dispensed
活性成分
    • fluticasone propionate 500.0 µg
    • salmeterol xinafoate 50.0 µg
剂型Inhalation powder, pre-dispensed
上市许可持有人APC Instytut Sp. z o.o. Al. Jerozolimskie 146C Warszawa 02-305 Poland
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Netherlands (NL)
      Salmeterol/Fluticasone APC 50 microgram/500 microgram/dosis inhalatiepoeder, voorverdeeld
    • Luxembourg (LU)
    • Italy (IT)
    • Romania (RO)
    • Malta (MT)
许可日期2018/09/28
最近更新日期2024/05/29
药物ATC编码
    • R03AK06 salmeterol and fluticasone
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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