欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
SE/H/1080/001
药品名称
Aprokam
活性成分
cefuroxime 50.0 mg
剂型
Powder for solution for injection
上市许可持有人
Laboratoires Théa France
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Germany (DE)
CEFCAM 50 mg Pulver zur Herstellung einer Injektionslösung
Denmark (DK)
Belgium (BE)
APROKAM 50 mg Powder for solution for injection
Netherlands (NL)
Luxembourg (LU)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Aprokam 50 mg Pulver zur Herstellung einer Injektionslösung
France (FR)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Norway (NO)
Finland (FI)
Aprokam 500 mg injektiokuiva-aine liuosta varten
Poland (PL)
Aprokam
Cyprus (CY)
CEFCAM PWD FOR SOL FOR INJ
Czechia (CZ)
Cefcam 50 mg
Romania (RO)
APROKAM 50 mg pulbere pentru soluţie injectabilă
Slovakia (SK)
APROCAM
Slovenia (SI)
许可日期
2012/04/25
最近更新日期
2022/12/15
药物ATC编码
S01AA Antibiotics
申请类型
TypeLevel1：
Known Active Substance
TypeLevel2：
Initial Application
TypeLevel3：
Bibliographic Art 10 a Dir 2001/83/EC
TypeLevel4：
Chemical Substance
TypeLevel5：
Prescription Only
附件文件下载
Final PL
|
SE/H/1080/001_Final PL
Date of last change:2014/01/15
Final SPC
|
SE/H/1080/001_Final SPC
Date of last change:2014/01/15
PAR
|
SE/H/1080/001_PAR
Date of last change:2014/01/15
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase