欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IT/H/0443/002
药品名称
Pramipexolo Sandoz GmbH 0,18 mg Compresse
活性成分
pramipexole 0.18 mg
剂型
Tablet
上市许可持有人
Sandoz GmbH Biochemiestrasse 10 6250 Kundl Austria
参考成员国 - 产品名称
Italy (IT)
互认成员国 - 产品名称
许可日期
2010/07/14
最近更新日期
2020/06/11
药物ATC编码
N04BC05 pramipexole
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
Final PL
|
Common PL Pramipexolo Sandoz GMBH _cl_
Date of last change:2024/09/06
Final SPC
|
Common SPC Pramipexolo Sandoz GMBH _cl_
Date of last change:2024/09/06
Final Labelling
|
Labelling
Date of last change:2024/09/06
Final Product Information
|
DE2385_Pramipexol_labelling_20131205_renewal
Date of last change:2024/09/06
Final Product Information
|
DE2385_Pramipexol_PL_20131205_renewal
Date of last change:2024/09/06
Final Product Information
|
DE2385_Pramipexol_SPC_20131205_renewal
Date of last change:2024/09/06
PubAR
|
PAREN_DE2385_2386_DC_Pramithon_Pexogies_20100921_final
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase