欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0896/002
药品名称
Epoprostenol Normon
活性成分
epoprostenol sodium salt 1.5 mg
剂型
Powder for solution for infusion
上市许可持有人
Laboratórios Normon, S.A.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2013/06/07
最近更新日期
2018/08/16
药物ATC编码
B01AC09 epoprostenol
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
附件文件下载
Final Product Information
|
common-spc-1500
Date of last change:2013/06/07
Final Product Information
|
common-outer-500
Date of last change:2013/06/07
Final Product Information
|
common-outer-1500
Date of last change:2013/06/07
Final Product Information
|
common-pl-500
Date of last change:2013/06/07
Final Product Information
|
common-pl-1500
Date of last change:2013/06/07
Final Product Information
|
common-spc-500
Date of last change:2013/06/07
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase