欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
EE/H/0240/001
药品名称
Memantine Grindeks
活性成分
memantine hydrochloride 10.0 mg
剂型
Film-coated tablet
上市许可持有人
AS GRINDEKS Krustpils iela 53 Rīga, LV-1057 Latvia
参考成员国 - 产品名称
Estonia (EE)
Tingreks
互认成员国 - 产品名称
Romania (RO)
Slovakia (SK)
Greece (GR)
Ireland (IE)
Austria (AT)
Latvia (LV)
Memantine Grindeks 10 mg apvalkotās tabletes
Lithuania (LT)
Memantine Grindeks 10 mg plėvele dengtos tabletės
France (FR)
Portugal (PT)
Poland (PL)
Croatia (HR)
Hungary (HU)
Memantine Grindeks
Italy (IT)
Czechia (CZ)
Memantine Grindeks
许可日期
2016/10/18
最近更新日期
2024/05/10
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 Labelling
|
common-outer
Date of last change:2016/11/24
Final Labelling
|
common-impack
Date of last change:2016/11/24
Final PL
|
common-pl
Date of last change:2016/11/24
Final SPC
|
common-spc
Date of last change:2016/11/24
PAR
|
20161124_PAR_memantine_MRI
Date of last change:2016/11/24
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase