欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IE/H/1262/002
药品名称
Rizadia 5mg Tablets
活性成分
Rizatriptan benzoate 5.0 mg
剂型
Tablet
上市许可持有人
Diapharm GmbH & Co. KG Hafenweg 18-20 48155 Münster Germany
参考成员国 - 产品名称
Ireland (IE)
互认成员国 - 产品名称
Germany (DE)
Rizadia 5 mg Tabletten
许可日期
2024/03/15
最近更新日期
2025/08/26
药物ATC编码
N02CC04 rizatriptan
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Informed Consent Art 10c Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
RIZADIA_IE_H_1262_001_002_IA_004_PI_EU_en_CRT _ 002
Date of last change:2025/08/12
PubAR Summary
|
Public Assessment Report
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase