欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/4347/001
药品名称
Levetiracetam Bluefish
活性成分
levetiracetam 250.0 mg
剂型
Film-coated tablet
上市许可持有人
Bluefish Pharmaceuticals AB Sweden
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Ireland (IE)
Spain (ES)
Portugal (PT)
许可日期
2011/09/30
最近更新日期
2017/01/05
药物ATC编码
N03AX14 levetiracetam
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
|
DE_H_4347_001_PAR
Date of last change:2024/09/06
Final Labelling
|
DE_4347_Levetiracetam Bluefish_Label_ Clean_20160901_renewal
Date of last change:2024/09/06
Final PL
|
DE_4347_Levetiracetam Bluefish_PIL _ Clean_20160901_renewal
Date of last change:2024/09/06
Final SPC
|
DE_4347_Levetiracetam Bluefish_PIL _ Clean_20160901_renewal_2
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase