欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0660/005
药品名称
Pramipexol Aurobindo
活性成分
pramipexole dihydrochloride 0.09 mg
剂型
Tablet
上市许可持有人
Aurobindo Pharma (Malta) Ltd.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Germany (DE)
Pramipexol Aurobindo 0,088 mg Tabletten
Denmark (DK)
Italy (IT)
Sweden (SE)
Malta (MT)
Pramipexole Aurobindo 0.088mg Tablets
许可日期
2012/04/03
最近更新日期
2024/08/27
药物ATC编码
N04BC05 pramipexole
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 PL
|
common_pl
Date of last change:2024/09/06
Final Product Information
|
common_pl_clean
Date of last change:2024/09/06
Final SPC
|
common_spc
Date of last change:2024/09/06
Final Product Information
|
common_spc_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase