欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
FR/V/0225/001
药品名称
Kesium 50
活性成分
amoxicillin trihydrate 40.0 mg
剂型
Tablet
上市许可持有人
Sogeval 200 route de mayenne BP 2227- 53022 LAVAL CEDEX
参考成员国 - 产品名称
France (FR)
KESIUM 50 13054
互认成员国 - 产品名称
Germany (DE)
Kesium 50 mg
Denmark (DK)
Belgium (BE)
Kesium 40 mg - 10 mg
Netherlands (NL)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Kesium 50 mg Chewable Tablets for Cats and Dogs
Ireland (IE)
Kesium 50 mg Chewable Tablets for cats and dogs
Austria (AT)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Sweden (SE)
Kesium
Finland (FI)
Poland (PL)
Hungary (HU)
Czechia (CZ)
Romania (RO)
许可日期
2011/06/22
最近更新日期
2024/07/12
药物ATC编码
QJ01CR02 amoxicillin and beta-lactamase inhibitor
申请类型
TypeLevel1：
[not specified]
TypeLevel2：
[not specified]
TypeLevel3：
Generic - art 13.2 Dir 2001/82/EC
TypeLevel4：
[not specified]
TypeLevel5：
[not specified]
附件文件下载
Final SPC
|
appendix_1_part_1b_kesium_250mg_tab_en_clean_version
Date of last change:2024/09/06
Final SPC
|
appendix_1_part_1b_kesium_500mg_tab_en_clean_version
Date of last change:2024/09/06
Final SPC
|
appendix_1_part_1b_kesium_50mg_tab_en_clean_version
Date of last change:2024/09/06
Final Product Information
|
appendix_1_part_1b_kesium_50mg_tab_en_clean_version_2
Date of last change:2024/09/06
Final SPC
|
appendix_1_part_1b_kesium_62_5mg_tab_en_clean_version
Date of last change:2024/09/06
Final SPC
|
appendix_1_part_1b_kesium_625mg_tab_en_clean_version
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase