欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
DK/H/0964/001
药品名称
Amlodipin Sandoz
活性成分
Amlodipine besilate 5.0 mg
剂型
Tablet
上市许可持有人
Sandoz A/S Edvard Thomsens Vej 14 2300 København S Denmark
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Belgium (BE)
Netherlands (NL)
United Kingdom (Northern Ireland) (XI)
Austria (AT)
Amlodipin Sandoz 5 mg - Tabletten
Spain (ES)
Italy (IT)
Greece (GR)
Sweden (SE)
Norway (NO)
Finland (FI)
Estonia (EE)
Czechia (CZ)
Slovakia (SK)
Slovenia (SI)
Portugal (PT)
Bulgaria (BG)
Amlopin
许可日期
2006/10/11
最近更新日期
2024/11/26
药物ATC编码
C08CA01 amlodipine
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 Labelling
|
1_3_1 spc_label_pl _ common_outer _ 456 _ clean
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_outer_clean _ 469
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_pl _ 12_907 clean
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_spc _ 12_445 clean
Date of last change:2024/09/06
Final PL
|
Amlodipin PIL common _ DK_H_0964_001_003_IA_114 _ clean
Date of last change:2024/09/06
Final SPC
|
Amlodipin SPC common _ DK_H_0964_001_003_IA_114 _ clean
Date of last change:2024/09/06
市场状态
Positive
©2006-2024
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European Union HMA Authorisation of Medicines DataBase