欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/0977/003
药品名称
Perindopril Ranbaxy 8 mg
活性成分
Perindopril tert-butylamine 8.0 mg
剂型
Tablet
上市许可持有人
Ranbaxy UK Ltd.
参考成员国 - 产品名称
Netherlands (NL)
35210
互认成员国 - 产品名称
Latvia (LV)
Perindobax 8 mg tabletes
Lithuania (LT)
Perindobax 8 mg tabletės
许可日期
2008/05/01
最近更新日期
2025/01/06
药物ATC编码
C09AA04 perindopril
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_combined_pl8mgclean
Date of last change:2025/01/06
Final SPC
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common_combined_spc4mgclean
Date of last change:2025/01/06
Final Product Information
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common_interpack_2mg_clean
Date of last change:2024/09/06
Final Labelling
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common_interpack_2mg_clean_2
Date of last change:2024/09/06
Final Product Information
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common_interpack_2mg_track changes
Date of last change:2024/09/06
Final Product Information
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common_interpack_4mg_clean
Date of last change:2024/09/06
Final Labelling
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common_interpack_4mg_clean_2
Date of last change:2024/09/06
Final Product Information
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common_interpack_4mg_track changes
Date of last change:2024/09/06
Final Product Information
|
common_interpack_8mg_clean
Date of last change:2024/09/06
Final Labelling
|
common_interpack_8mg_clean_2
Date of last change:2024/09/06
Final Product Information
|
common_interpack_8mg_track changes
Date of last change:2024/09/06
Final Product Information
|
common_pl_2mg_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_2mg_track changes
Date of last change:2024/09/06
Final Product Information
|
common_pl_4mg_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_4mg_track changes
Date of last change:2024/09/06
Final Product Information
|
common_pl_8mg_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_8mg_track changes
Date of last change:2024/09/06
Final Product Information
|
common_spc_2mg_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_2mg_track changes
Date of last change:2024/09/06
Final Product Information
|
common_spc_4mg_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_4mg_track changes
Date of last change:2024/09/06
Final Product Information
|
common_spc_8mg_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_8mg_track changes
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase