欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PL/H/0784/002
药品名称
Ospamox
活性成分
amoxicillin trihydrate 750.0 mg
剂型
Film-coated tablet
上市许可持有人
Sandoz GmbH
参考成员国 - 产品名称
Poland (PL)
互认成员国 - 产品名称
许可日期
2009/08/27
最近更新日期
2023/12/29
药物ATC编码
J01CA04 amoxicillin
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
Final SPC
|
final_common_SPC_AT_H_0188_003-006_IB_022_clean
Date of last change:2020/02/17
Final SPC
|
final_common_SPC_AT_H_0188_001-003_IB_022_clean
Date of last change:2020/02/17
Final Labelling
|
final_common_LAB_AT_H_0188_001-003_IB_022_clean
Date of last change:2020/02/17
Final Labelling
|
final_common_LAB_AT_H_0188_003-006_IB_022_clean
Date of last change:2020/02/17
Final PL
|
final_common_PIL_AT_H_0188_001-003_IB_022_clean
Date of last change:2020/02/17
Final PL
|
final_common_PIL_AT_H_0188_003-006_IB_022_clean
Date of last change:2020/02/17
PAR
|
PAR_AT_H_188_001-006_Amoxicillin Hexal Filmtabletten
Date of last change:2017/05/18
Final Product Information
|
PIL 01-03
Date of last change:2013/02/20
Final Product Information
|
PIL 04-06
Date of last change:2013/02/20
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase