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

MR编号	DE/H/6056/004
药品名称	Levetiracetam Holsten 1000 mg Filmtabletten
活性成分	levetiracetam 1000.0 mg
剂型	Film-coated tablet
上市许可持有人	Holsten Pharma GmbH Hahnstraße 31-35 DE-60528 Frankfurt am Main Germany
参考成员国 - 产品名称	Germany (DE) Levetiracetam Holsten 1000 mg Filmtabletten
互认成员国 - 产品名称	France (FR) Greece (GR) Italy (IT) Spain (ES)
许可日期	2018/11/16
最近更新日期	2024/05/15
药物ATC编码	N03AX14 levetiracetam
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 \| 2183890_93_PAREN_DE 6056_LevetiracetamDate of last change:2024/09/06 Final Product Information \| common_final_pl_6056_001__V006Date of last change:2024/09/06 Final Product Information \| common_final_pl_6056_002__V006Date of last change:2024/09/06 Final Product Information \| common_final_pl_6056_003__V006Date of last change:2024/09/06 Final Product Information \| common_final_pl_6056_004__V006Date of last change:2024/09/06 Final Product Information \| common_final_spc_6056_001__V006Date of last change:2024/09/06 Final Product Information \| common_final_spc_6056_002__V006Date of last change:2024/09/06 Final Product Information \| common_final_spc_6056_003__V006Date of last change:2024/09/06 Final Product Information \| common_final_spc_6056_004__V006Date of last change:2024/09/06 Final Labelling \| final_common_lab_DE_H_6056_004_IA_014Date of last change:2024/09/06 Final PL \| final_common_pl_6056_004__015Date of last change:2024/09/06 Final SPC \| final_common_spc_6056_004__015Date of last change:2024/09/06
市场状态	Positive