欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
CZ/H/0876/003
药品名称
MEDOPEXOL
活性成分
pramipexole 700.0 µg
剂型
Tablet
上市许可持有人
Medochemie Ltd. 1-10 Constantinoupoleus street 3011, Limassol Cyprus
参考成员国 - 产品名称
Czechia (CZ)
互认成员国 - 产品名称
Greece (GR)
Latvia (LV)
Medopexol 0,7 mg tabletes
Lithuania (LT)
MEDOPEXOL 0,7 mg tabletės
Bulgaria (BG)
Apeiron
Cyprus (CY)
APEIRON 0,7mg TABS
Romania (RO)
MEDOPEXOL 0,7 mg, comprimate
Slovakia (SK)
MEDOPEXOL 0,7 mg
许可日期
2009/06/10
最近更新日期
2023/02/02
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 Product Information
|
common_combined_pilmay2022_clean
Date of last change:2022/07/09
Final SPC
|
common-combined-spcapr2020-clean
Date of last change:2020/06/15
Final PL
|
common-combined-pilapr2020-clean
Date of last change:2020/06/15
Final Labelling
|
Labelling Medopexol EN
Date of last change:2016/01/26
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase