欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/V/0225/003
药品名称
Kesium 250
活性成分
amoxicillin trihydrate 200.0 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 250 13056
互认成员国 - 产品名称
Germany (DE)
Kesium 250 mg
Denmark (DK)
Belgium (BE)
Kesium 200 mg - 50 mg
Netherlands (NL)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Kesium 250 mg Chewable Tablets for Cats and Dogs
Ireland (IE)
Kesium 250 mg Chewable Tablets for 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
|
ap_1_part_1b_kesium_250_mg_tab_clean_en_version
Date of last change:2024/09/06
市场状态
Positive
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