欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/2087/001
药品名称
Clarithromycin 250 mg
活性成分
clarithromycin 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
Belgium (BE)
Spain (ES)
Poland (PL)
Bulgaria (BG)
Clarithromycin Sandoz
Romania (RO)
Claritromicina Sandoz 250 mg comprimate filmate
Slovakia (SK)
LEKOKLAR 250 mg filmom obalené tablety
许可日期
2011/08/29
最近更新日期
2024/08/22
药物ATC编码
J01FA09 clarithromycin
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
common_pl_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_clean
Date of last change:2024/09/06
PubAR
|
PAR_2087_DC_claritromycine_17 nov 2011
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase