欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/0918/003
药品名称
Polaris
活性成分
memantine hydrochloride 5.0 mg
memantine hydrochloride 10.0 mg
memantine hydrochloride 15.0 mg
memantine hydrochloride 20.0 mg
剂型
Film-coated tablet
上市许可持有人
Pharmanel Commercial Pharmaceuticals, S.A.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
许可日期
2014/02/13
最近更新日期
2018/07/19
药物ATC编码
N06DX01 memantine
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
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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
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common_outer 20mg
Date of last change:2024/09/06
Final Product Information
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common_outer_2
Date of last change:2024/09/06
Final Product Information
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common_outer_combinationpack
Date of last change:2024/09/06
Final Product Information
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common_pl
Date of last change:2024/09/06
Final Product Information
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common_pl_2
Date of last change:2024/09/06
Final Product Information
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common_pl_combinationpack
Date of last change:2024/09/06
Final Product Information
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common_pl10mg
Date of last change:2024/09/06
Final Product Information
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common_pl20mg
Date of last change:2024/09/06
Final Product Information
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common_spc
Date of last change:2024/09/06
Final Product Information
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common_spc_2
Date of last change:2024/09/06
Final Product Information
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common_spc_combinationpack
Date of last change:2024/09/06
Final Product Information
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common_spc10mg
Date of last change:2024/09/06
Final Product Information
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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