欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	DE/H/3652/003
药品名称	Memantin Heumann 5 mg Filmtabletten Memantin Heumann 10 mg Filmtabletten Memantin Heumann 15 mg Filmtabletten Memantin Heumann 20 mg Filmtabletten
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	Heumann Pharma GmbH & Co. Generica KG Südwestpark 50 D-90449 Nürnberg
参考成员国 - 产品名称	Germany (DE) Memantin Heumann 5mg / 10 mg / 15 mg / 20 mg Filmtabletten Starterpacket
互认成员国 - 产品名称	Greece (GR)
许可日期	2013/02/18
最近更新日期	2024/05/23
药物ATC编码	N06DX01 memantine
申请类型	TypeLevel1：Abridged TypeLevel2：Additional Strength/Form 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 \| common-final-labip-3652-V013Date of last change:2020/02/14 Final Product Information \| common-final-labop-3652-V013Date of last change:2020/02/14 Final Product Information \| common-final-pl-3652-V013Date of last change:2020/02/14 Final Product Information \| common-final-spc-3652-V013Date of last change:2020/02/14 Final PL \| DE_3652_Memantin_pl_clean_20171120_renewalDate of last change:2019/02/07 Final SPC \| DE_3652_Memantin_spc_clean_20171120_renewalDate of last change:2019/02/07 Final Labelling \| DE_3652_Memantin_outer_clean_20171120_renewalDate of last change:2019/02/07 Final Labelling \| DE_3652_Memantin_impack_clean_20171120_renewalDate of last change:2019/02/07 PAR \| PAREN-DE3652_Memantin Heumann-20140122Date of last change:2014/01/22
市场状态	Positive