欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
EE/H/0313/002
药品名称
Atsimutin
活性成分
azathioprine 50.0 mg
剂型
Film-coated tablet
上市许可持有人
Bausch Health Ireland Limited 3013 Lake Drive Dublin 24 Co. Dublin Ireland
参考成员国 - 产品名称
Estonia (EE)
Atsimutin
互认成员国 - 产品名称
Lithuania (LT)
Atsimutin 50 mg plėvele dengtos tabletės
Latvia (LV)
Atsimutin 50 mg apvalkotās tabletes
Czechia (CZ)
Atioprin 50 mg potahované tablety
Slovakia (SK)
许可日期
2013/03/14
最近更新日期
2023/03/31
药物ATC编码
L04AX01 azathioprine
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
PubAR
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04_DEH30367901_02 Azathioprin_Pharma_Resources_final PAR
Date of last change:2024/09/06
Final PL
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1_3_1_pal_en_aza_25mg_common_de_h_3037_001_dc
Date of last change:2024/09/06
Final PL
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1_3_1_pal_en_aza_25mg_common_de_h_3037_001_dc_clean
Date of last change:2024/09/06
Final PL
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1_3_1_pal_en_aza_50mg_common_de_h_3037_002_dc
Date of last change:2024/09/06
Final PL
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1_3_1_pal_en_aza_50mg_common_de_h_3037_002_dc_clean
Date of last change:2024/09/06
Final SPC
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1_3_1_smpc_common_en_azathioprine_aqvida_25mg_DE_H_3037_001_DC
Date of last change:2024/09/06
Final SPC
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1_3_1_smpc_common_en_azathioprine_aqvida_25mg_DE_H_3037_001_DC_clean
Date of last change:2024/09/06
Final SPC
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1_3_1_smpc_common_en_azathioprine_aqvida_50mg_DE_H_3037_001_DC
Date of last change:2024/09/06
Final SPC
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1_3_1_smpc_common_en_azathioprine_aqvida_50mg_DE_H_3037_001_DC_clean
Date of last change:2024/09/06
Final Product Information
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common_final_labip_3037_0012__V012
Date of last change:2024/09/06
Final Product Information
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common_final_labip_3037_002__V012
Date of last change:2024/09/06
Final Product Information
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common_final_labop_3037_001__V012
Date of last change:2024/09/06
Final Product Information
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common_final_labop_3037_002__V012
Date of last change:2024/09/06
Final Product Information
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common_final_pl_3037_001__V012
Date of last change:2024/09/06
Final Product Information
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common_final_pl_3037_002__V012
Date of last change:2024/09/06
Final Product Information
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common_final_spc_3037_001__V012
Date of last change:2024/09/06
Final Product Information
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common_final_spc_3037_002__V012
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase