欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/3043/004
药品名称
Topiramate 200 mg film-coated tablets
活性成分
topiramate 200.0 mg
剂型
Film-coated tablet
上市许可持有人
Aristo Pharma GmbH
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
许可日期
2010/04/28
最近更新日期
2024/01/02
药物ATC编码
N03AX11 topiramate
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
|
common_LAB_3043_clean
Date of last change:2024/09/06
Final Product Information
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common_labip_ET_topiramat_25mg_50mg_100mg_200mg_fct_V01_0819_cl
Date of last change:2024/09/06
Final Product Information
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common_labip_FO_topiramat_25mg_50mg_100mg_200mg_fct_V01_0819_cl
Date of last change:2024/09/06
Final Product Information
|
common_labop_topiramat_25mg_50mg_100mg_200mg_fct_V01_0819_cl
Date of last change:2024/09/06
Final PL
|
common_pl_topiramat_25mg_50mg_100mg_200mg_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_topiramat_25mg_50mg_100mg_200mg_fct_V01_0919_cl
Date of last change:2024/09/06
Final SPC
|
common_spc_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_topiramat_25mg_50mg_100mg_200mg_fct_V01_0819_cl
Date of last change:2024/09/06
市场状态
Withdrawn(注:已撤市)
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European Union HMA Authorisation of Medicines DataBase