欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1125/004
药品名称
Levebon
活性成分
levetiracetam 1000.0 mg
剂型
Film-coated tablet
上市许可持有人
G.L. Pharma GmbH Austria
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Austria (AT)
Levetiracetam G.L. 1000 mg Filmtabletten
Poland (PL)
Levebon
Bulgaria (BG)
Levebon
Czechia (CZ)
Levetiracetam G.L. Pharma 1000 mg potahované tablety
许可日期
2012/01/17
最近更新日期
2023/10/05
药物ATC编码
N03AX14 levetiracetam
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
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
|
SE_H_1125_004_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_1125_004_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_1125_004_PAR
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase