欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NO/H/0319/001
药品名称
Ampicillin
活性成分
Ampicillin sodium 2.0 g
剂型
Powder for solution for injection/infusion
上市许可持有人
Antibiotice S.A.
参考成员国 - 产品名称
Norway (NO)
互认成员国 - 产品名称
Czechia (CZ)
Amroliv 500 mg powder for solution for injection/infusion
Germany (DE)
Spain (ES)
Denmark (DK)
Poland (PL)
Finland (FI)
许可日期
2022/02/17
最近更新日期
2024/11/18
药物ATC编码
J01CA01 ampicillin
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial 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
|
Amroliv_common_pl
Date of last change:2024/09/06
Final SPC
|
Amroliv_common_spc
Date of last change:2024/09/06
PubAR
|
PAR Amroliv
Date of last change:2024/09/06
PubAR Summary
|
Summary PAR Amroliv
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase