欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0896/001
药品名称
Epoprostenol Normon
活性成分
epoprostenol sodium salt 0.5 mg
剂型
Powder and solvent 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_outer_1500
Date of last change:2024/09/06
Final Product Information
|
common_outer_500
Date of last change:2024/09/06
Final Product Information
|
common_pl_1500
Date of last change:2024/09/06
Final Product Information
|
common_pl_500
Date of last change:2024/09/06
Final Product Information
|
common_spc_1500
Date of last change:2024/09/06
Final Product Information
|
common_spc_500
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase