欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/0869/001
药品名称
Acarbose dura 50 mg Tabletten
活性成分
acarbose 50.0 mg
剂型
Tablet
上市许可持有人
Mylan Germany GmbH Lütticher Straße 5 53842 Troisdorf Germany
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Spain (ES)
Portugal (PT)
Italy (IT)
许可日期
2008/09/11
最近更新日期
2024/06/18
药物ATC编码
A10BF01 acarbose
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
PubAR
|
04_DE_0869_0870_0936_0937_1_2_DC Acarbose_final PAR
Date of last change:2024/09/06
Final Product Information
|
common_combined_de0869_clean_v02
Date of last change:2024/09/06
Final Product Information
|
common_combined_de0869_tracked_v
Date of last change:2024/09/06
Final Labelling
|
DE_H_869_870_936_937_01_2_DC_ Acarbose D210 _ Lab
Date of last change:2024/09/06
Final PL
|
DE_H_869_870_936_937_01_2_DC_ Acarbose D210 _ PIL
Date of last change:2024/09/06
Final SPC
|
DE_H_869_870_936_937_01_2_DC_ Acarbose D210 _ SPC
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase