欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/V/0153/001
药品名称
Vetrimoxin L.A. 150 mg/ml
活性成分
amoxicillin trihydrate 150.0 mg/ml
剂型
Suspension for injection
上市许可持有人
Ceva Tiergesundheit GmbH
参考成员国 - 产品名称
Germany (DE)
Vetrimox L.A. 150 mg/ ml
互认成员国 - 产品名称
Denmark (DK)
Netherlands (NL)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Vetrimoxin L.A.
Ireland (IE)
Longocilline 150 mg/ml Suspension for Injection for Cattle & Pigs
Austria (AT)
Sweden (SE)
Finland (FI)
许可日期
2012/11/22
最近更新日期
2023/04/24
药物ATC编码
QJ01CA04 amoxicillin
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 PL
|
2401205_palen_20141126
Date of last change:2024/09/06
PubAR
|
2401205_paren_20130213
Date of last change:2024/09/06
Final SPC
|
2401205_spcen_20141126
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase