欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/3043/001
药品名称
Topiramate 25 mg film-coated tablets
活性成分
topiramate 25.0 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
2024/02/14
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_labip_ET_topiramat_25mg_50mg_fct_V02_1223_Clean _ TTL OK
Date of last change:2024/04/06
Final PL
|
common_pl_topiramat_25mg_50mg_fct_V04_1223_Clean _ TTL OK
Date of last change:2024/04/06
Final SPC
|
common_spc_topiramat_25mg_50mg_fct_V05_1223_Clean _ TTL OK
Date of last change:2024/04/06
Final Product Information
|
common-labop-topiramat-25mg_50mg_100mg_200mg_fct-V01-0819-cl
Date of last change:2019/10/31
Final Product Information
|
common-labip-ET-topiramat-25mg_50mg_100mg_200mg_fct-V01-0819-cl
Date of last change:2019/10/31
Final Product Information
|
common-labip-FO-topiramat-25mg_50mg_100mg_200mg_fct-V01-0819-cl
Date of last change:2019/10/31
Final Product Information
|
common-pl-topiramat-25mg_50mg_100mg_200mg-fct-V01-0919-cl
Date of last change:2019/10/31
Final Product Information
|
common-spc-topiramat-25mg_50mg_100mg_200mg-fct-V01-0819-cl
Date of last change:2019/10/31
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase