欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1335/007
药品名称
Pregabalina Lupin
活性成分
pregabalin 225.0 mg
剂型
Capsule, hard
上市许可持有人
Lupin (Europe) Limited
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2015/08/12
最近更新日期
2018/09/14
药物ATC编码
N03AX16 pregabalin
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 Product Information
|
131_blister
Date of last change:2024/09/06
Final Product Information
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131_carton
Date of last change:2024/09/06
Final Product Information
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131_label
Date of last change:2024/09/06
Final Product Information
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131_leaflet
Date of last change:2024/09/06
Final Product Information
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131_spc
Date of last change:2024/09/06
PubAR
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589321_589326_589324_589322_589325_589328_589327_589323_PAR_GBB
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase