欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
NL/H/0343/003
药品名称
Crestor 40 mg
活性成分
Rosuvastatin 40.0 mg
剂型
Film-coated tablet
上市许可持有人
Grünenthal B.V. De Corridor 21K 3621 ZA Breukelen The Netherlands
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Denmark (DK)
Belgium (BE)
Luxembourg (LU)
Ireland (IE)
Austria (AT)
Crestor 40 mg - Filmtabletten
Portugal (PT)
Italy (IT)
Greece (GR)
Sweden (SE)
Finland (FI)
Norway (NO)
许可日期
2003/03/07
最近更新日期
2024/12/02
药物ATC编码
C10AA07 rosuvastatin
申请类型
TypeLevel1：
New Active Substance
TypeLevel2：
Initial Application
TypeLevel3：
Full Dossier Article 4.8 Di 65/65
TypeLevel4：
Chemical Substance
TypeLevel5：
Prescription Only
附件文件下载
Final Labelling
|
Annex 1Label QRD _Crestor 10 mg_
Date of last change:2024/09/06
Final PL
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common PIL
Date of last change:2024/09/06
Final SPC
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common SmPC
Date of last change:2024/09/06
Final Product Information
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common_comb_crestor_annot_Avara_to_AZReims_Brecon_delet
Date of last change:2024/09/06
Final Product Information
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common_comb_crestor_clean_Avara_to_AZReims_Brecon_delet
Date of last change:2024/09/06
Final Product Information
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common_comb_provisacor_annot_Avara_to_AZReims_Brecon_delet
Date of last change:2024/09/06
Final Product Information
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common_comb_provisacor_clean_Avara_to_AZReims_Brecon_delet
Date of last change:2024/09/06
Final Product Information
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common_comb_rosuvastatin_annot_Avara_to_AZReims_Brecon_delet
Date of last change:2024/09/06
Final Product Information
|
common_comb_rosuvastatin_clean_Avara_to_AZReims_Brecon_delet
Date of last change:2024/09/06
PubAR
|
EPAR_CRESTOR_343_3 feb 2012_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