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

MR编号	AT/H/0187/003
药品名称	Amoxicillin Sandoz 1000 mg - Filmtabletten
活性成分	amoxicillin trihydrate 750.0 mg
剂型	Film-coated tablet
上市许可持有人	Sandoz GmbH Biochemiestrasse 10 6250 Kundl Austria
参考成员国 - 产品名称	Austria (AT) Amoxicillin Sandoz 1000 mg - Filmtabletten
互认成员国 - 产品名称	Denmark (DK) Slovakia (SK) Italy (IT) Latvia (LV) Ospamox 1000 mg apvalkotās tabletes Lithuania (LT) Ospamox 1000 mg plėvele dengtos tabletės Estonia (EE) Romania (RO) AMOXICILINA SANDOZ 1000 mg, comprimate filmate
许可日期	2009/10/29
最近更新日期	2024/01/02
药物ATC编码	J01CA04 amoxicillin
申请类型	TypeLevel1：Abridged TypeLevel2：Multiple (Copy) Application TypeLevel3：Other Generic application Art 10.3 Dir 2001/83/EC TypeLevel4：Chemical Substance TypeLevel5：Prescription Only
附件文件下载	Final PL \| common_PL_AT_H_0187_001-003_IB_025_cleanDate of last change:2020/02/17 Final SPC \| common_SPC_AT_H_0187_004-006_IB_025_cleanDate of last change:2020/02/17 Final SPC \| common_SPC_AT_H_0187_001-003_IB_025_cleanDate of last change:2020/02/17 Final Labelling \| common_LAB_AT_H_0187_001-003_IB_025_cleanDate of last change:2020/02/17 Final PL \| common_PL_AT_H_0187_003-006_IB_025_cleanDate of last change:2020/02/17 Final Labelling \| common_LAB_AT_H_0187_003-006_IB_025_cleanDate of last change:2020/02/17 PAR \| PAR_AT_H_187_001-006_Amoxicillin Sandoz FilmtablettenDate of last change:2017/05/18 Final Product Information \| PIL 01-03Date of last change:2013/02/20 Final Product Information \| PIL 04-06Date of last change:2013/02/20
市场状态	Positive