欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
ES/H/0262/001
药品名称
ROPRIMA 2 mg
活性成分
ropinirole hydrochloride 2.28 mg
剂型
Prolonged-release tablet
上市许可持有人
TEVA GmbH Graf-Arco-Str. 3 D-89079 Ulm
参考成员国 - 产品名称
Spain (ES)
互认成员国 - 产品名称
许可日期
2011/02/04
最近更新日期
2023/06/22
药物ATC编码
N04BC04 ropinirole
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 Labelling
|
DE2716_Roprima_ label_inner_eu clean_20140219_renewal
Date of last change:2024/09/06
Final Labelling
|
DE2716_Roprima_label_outer_eu clean_20140219_renewal
Date of last change:2024/09/06
Final PL
|
DE2716_Roprima_pil_eu clean_20140219_renewal
Date of last change:2024/09/06
Final SPC
|
DE2716_Roprima_SmpC_clean_20140219_renewal
Date of last change:2024/09/06
PubAR
|
PAREN_DE2124_2716_2717_2718_Ropinirol Krka_20110415_final
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase