欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PL/H/0598/003
药品名称
Polmatine
活性成分
memantine hydrochloride 5.0 mg
剂型
Oral solution
上市许可持有人
Medana Pharma SA 10 Władysława Łokietka Street 98-200 Sieradz Poland
参考成员国 - 产品名称
Poland (PL)
互认成员国 - 产品名称
Bulgaria (BG)
Polmatine
许可日期
2013/05/20
最近更新日期
2021/06/16
药物ATC编码
N06DX01 memantine
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
PubAR
|
EE_H_183_001_003_DC_PublicAR
Date of last change:2024/09/06
Final PL
|
PI_sol
Date of last change:2024/09/06
Final Product Information
|
2020_10_07_ PIL_Memantine_5mg_oral solution_2020_09EN_track_ OLD
Date of last change:2024/09/06
Final SPC
|
2020_10_07_ SmPC_Memantine_5mg_oral solution_2020_09EN_track_ OLD
Date of last change:2024/09/06
Final Labelling
|
LB_Memantine_5 mg_oral solution_2020_05EN_track
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase