欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
DE/H/4808/001
药品名称
Ralenova 2 mg/ml
活性成分
Mitoxantrone hydrochloride 2.0 mg/ml
剂型
Solution for injection
上市许可持有人
MEDA Pharma GmbH&Co.KG Benzstrasse 1 61352 Bad Homburg Germany
参考成员国 - 产品名称
Germany (DE)
Ralenova 2 mg/ml
互认成员国 - 产品名称
France (FR)
Spain (ES)
Norway (NO)
许可日期
2016/08/03
最近更新日期
2024/12/03
药物ATC编码
L01DB07 mitoxantrone
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
Final Product Information
|
common_final_labop_4808_001__V007G
Date of last change:2024/09/06
Final Product Information
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common_final_labop_4808_002__V007G
Date of last change:2024/09/06
Final Product Information
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common_final_labop_4808_003__V007G
Date of last change:2024/09/06
Final Product Information
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common_final_pl_4808_001__V007G
Date of last change:2024/09/06
Final Product Information
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common_final_pl_4808_002__V007G
Date of last change:2024/09/06
Final Product Information
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common_final_pl_4808_003__V007G
Date of last change:2024/09/06
Final Product Information
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common_final_spc_4808_001__V007G
Date of last change:2024/09/06
Final Product Information
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common_final_spc_4808_002__V007G
Date of last change:2024/09/06
Final Product Information
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common_final_spc_4808_003__V007G
Date of last change:2024/09/06
Final PL
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Patient Information Leaflet_10mg_V010RTQ_common
Date of last change:2024/09/06
Final PL
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Patient Information Leaflet_10mg_V010RTQ_common_annotated
Date of last change:2024/09/06
Final PL
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Patient Information Leaflet_20mg_V010RTQ_common
Date of last change:2024/09/06
Final PL
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Patient Information Leaflet_20mg_V010RTQ_common_annotated
Date of last change:2024/09/06
Final PL
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Patient Information Leaflet_2mg_V010RTQ_common
Date of last change:2024/09/06
Final PL
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Patient Information Leaflet_2mg_V010RTQ_common_annotated
Date of last change:2024/09/06
Final SPC
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SmPC_10 mg_V010RTQ_common
Date of last change:2024/09/06
Final SPC
|
SmPC_10 mg_V010RTQ_common_annotated
Date of last change:2024/09/06
Final SPC
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SmPC_2 mg_V010RTQ_common
Date of last change:2024/09/06
Final SPC
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SmPC_2 mg_V010RTQ_common_annotated
Date of last change:2024/09/06
Final SPC
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SmPC_20 mg_V010RTQ_common
Date of last change:2024/09/06
Final SPC
|
SmPC_20 mg_V010RTQ_common_annotated
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase