欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
EL/H/0342/001
药品名称
ZOLMEMIN
活性成分
Memantine hydrochloride 10.0 mg
剂型
Film-coated tablet
上市许可持有人
VIAN S.A. 2, Ag. Nektariou str. 153 44 Gerakas, Pallini, Attica, Greece
参考成员国 - 产品名称
Greece (GR)
互认成员国 - 产品名称
许可日期
2014/02/13
最近更新日期
2025/01/03
药物ATC编码
N06DX01 memantine
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
|
56358_56361_56352_56364_20120212_PAR_GBB
Date of last change:2024/09/06
PubAR
|
56365_20150212_PAR_GBB
Date of last change:2024/09/06
Final Product Information
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common_impack
Date of last change:2024/09/06
Final Product Information
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common_impack 10mg
Date of last change:2024/09/06
Final Product Information
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common_impack 20mg
Date of last change:2024/09/06
Final Product Information
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common_impack_2
Date of last change:2024/09/06
Final Product Information
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common_impack_combinationpack
Date of last change:2024/09/06
Final Product Information
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common_outer
Date of last change:2024/09/06
Final Product Information
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common_outer 10mg
Date of last change:2024/09/06
Final Product Information
|
common_outer 20mg
Date of last change:2024/09/06
Final Product Information
|
common_outer_2
Date of last change:2024/09/06
Final Product Information
|
common_outer_combinationpack
Date of last change:2024/09/06
Final Product Information
|
common_pl
Date of last change:2024/09/06
Final Product Information
|
common_pl_2
Date of last change:2024/09/06
Final Product Information
|
common_pl_combinationpack
Date of last change:2024/09/06
Final Product Information
|
common_pl10mg
Date of last change:2024/09/06
Final Product Information
|
common_pl20mg
Date of last change:2024/09/06
Final Product Information
|
common_spc
Date of last change:2024/09/06
Final Product Information
|
common_spc_2
Date of last change:2024/09/06
Final Product Information
|
common_spc_combinationpack
Date of last change:2024/09/06
Final Product Information
|
common_spc10mg
Date of last change:2024/09/06
Final Product Information
|
common_spc20mg
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase