欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0805/002
药品名称
Recikalc-D forte
活性成分
calcium 500.0 mg
colecalciferol 800.0 IU
剂型
Chewable tablet
上市许可持有人
Viatris AB, Sweden
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Czechia (CZ)
Kalcipos-D forte 500 mg/800 IU
Denmark (DK)
Kalcipos-D
Netherlands (NL)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Calciduran Vit. D3 500 mg/800 I.E. - Kautabletten
Norway (NO)
Kalcipos-D forte
Finland (FI)
Slovakia (SK)
Kombi-Kalz 500 mg/800 IU žuvacie tablety
许可日期
2009/12/22
最近更新日期
2024/01/09
药物ATC编码
A12AX Calcium, combinations with vitamin D and/or other drugs
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Bibliographic Art 10 a Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
SE/H/0805/002_Final PL
Date of last change:2014/01/15
Final SPC
|
SE/H/0805/002_Final SPC
Date of last change:2014/01/15
PAR
|
SE/H/0805/002_PAR
Date of last change:2014/01/15
市场状态
Positive
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