欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
NL/H/0556/002
药品名称
Cefuroximaxetil 250
活性成分
cefuroxime 250.0 mg
剂型
Film-coated tablet
上市许可持有人
Sandoz B.V. Hospitaaldreef 29 1315 RC Almere Nederland
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Spain (ES)
Latvia (LV)
Belgium (BE)
United Kingdom (Northern Ireland) (XI)
Austria (AT)
Cefuroxim Sandoz 250 mg-Filmtabletten
Poland (PL)
Hungary (HU)
Czechia (CZ)
Slovakia (SK)
Lithuania (LT)
许可日期
2005/01/26
最近更新日期
2024/08/21
药物ATC编码
J01DA06 Cefuroxime
申请类型
TypeLevel1：
Abridged
TypeLevel2：
Additional Strength/Form
TypeLevel3：
Generic [Article 10.1.(a)(iii), first paragraph]
TypeLevel4：
Chemical Substance
TypeLevel5：
Prescription Only
附件文件下载
Final Labelling
|
1_3_1 spc_label_pl _ common_outer _ 2_995 clean
Date of last change:2024/09/06
Final Labelling
|
1_3_1 spc_label_pl _ common_outer _ 2_995 tracked
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_outer _ cl
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_pl _ cl
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_spc _ cl
Date of last change:2024/09/06
Final PL
|
common_pl_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_clean
Date of last change:2024/09/06
市场状态
Positive
©2006-2024
Drugfuture
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European Union HMA Authorisation of Medicines DataBase