欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号IE/H/0803/001
药品名称Plasma-Lyte 148 (pH 7.4) Solution for Infusion
活性成分
    • sodium chloride sodium gluconate 7.4 %
剂型Solution for infusion
上市许可持有人Baxter Healthcare, Caxton Way, Thetford, Norfolk, 1P24 3SE, United Kingdom
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)
      PL 00116/0332 - 0064
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
    • Iceland (IS)
    • Austria (AT)
      Plasmalyt - Infusionslösung
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
    • Lithuania (LT)
    • Czechia (CZ)
    • Netherlands (NL)
    • Slovakia (SK)
    • Italy (IT)
    • Greece (GR)
    • Cyprus (CY)
      PLASMA-LYTE
    • Slovenia (SI)
    • Croatia (HR)
    • Malta (MT)
许可日期2008/04/05
最近更新日期2023/12/15
药物ATC编码
    • B05BB02 electrolytes with carbohydrates
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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