欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
DE/H/8333/004
药品名称
Atolipidrin 40 mg - Filmtabletten
活性成分
Atorvastatin 40.0 mg
剂型
Film-coated tablet
上市许可持有人
Hexal AG Industriestrasse 25 83607 Holzkirchen Germany
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
许可日期
2009/06/10
最近更新日期
2025/10/23
药物ATC编码
C10AA05 atorvastatin
申请类型
TypeLevel1：
TypeLevel2：
TypeLevel3：
TypeLevel4：
TypeLevel5：
附件文件下载
Final PL
|
DE_H_8333_1_2_4_IA_056 Patient Information Leaflet for Variation IA 056
Date of last change:2025/06/11
Final SPC
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DE_H_8333_1_2_4_IA_056 Summary of Product Characteristics for Variation IA 056
Date of last change:2025/06/11
PubAR
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AT_H_0196_198_209_210_01_04_publicAR_final
Date of last change:2024/09/06
Final Product Information
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FRAR PIL AT_0196_0197_001_004_R_001_clean
Date of last change:2024/09/06
Final Product Information
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FRAR PIL AT_0198_001_004_R_001_clean
Date of last change:2024/09/06
Final Product Information
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FRAR SmPC AT_0196_0197_001_004_R_001_clean
Date of last change:2024/09/06
Final Product Information
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FRAR SmPC AT_0198_001_004_R_001_clean
Date of last change:2024/09/06
Final Product Information
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FRAR_LAB_AT_H_0196_0197_001_004_R_001_clean
Date of last change:2024/09/06
Final Product Information
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FRAR_LAB_AT_H_0198_001_004_R_001_clean
Date of last change:2024/09/06
Final Labelling
|
LAB_final_AT_H_0196_197_198_II_035_034_026_G_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase