欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0918/004
药品名称
Numeta G13E
活性成分
alanine 4.66 g
arginine 4.89 g
aspartic acid 3.5 g
calcium chloride dihydrate 3.45 g
cysteine 1.1 g
glucose monohydrate 550.0 g
glutamic acid 5.83 g
glycine 2.33 g
histidine 2.21 g
isoleucine 3.9 g
leucine 5.83 g
lysine 6.41 g
MAGNESIUM ACETATE tetrahydrate 0.63 g
methionine 1.4 g
ornithine 1.45 g
phenylalanine 2.45 g
potassium acetate 3.83 g
proline 1.75 g
serine 2.33 g
sodium glycerophosphate hydrate 6.15 g
taurine 0.35 g
threonine 2.16 g
tryptophan 1.17 g
tyrosine 0.45 g
valine 4.43 g
剂型
Emulsion for infusion
上市许可持有人
Baxter Medical AB Sweden
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Germany (DE)
Numeta G 13 % E
Denmark (DK)
Numeta G13E
Netherlands (NL)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Numeta G 13 % E Emulsion zur Infusion
France (FR)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
NUMETA® PRETERM
Norway (NO)
Numeta G13E
Finland (FI)
Poland (PL)
NUMETA G13% E Preterm
Czechia (CZ)
Numeta G13%E
Malta (MT)
Belgium (BE)
Numetzah G13%E émulsion pour perfusion
许可日期
2016/03/15
最近更新日期
2024/01/16
药物ATC编码
B05BA10 combinations
申请类型
TypeLevel1:
Line Extension
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Fixed combination Art 10b Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
PAR Summary
|
SE/H/0918/004_PAR Summary
Date of last change:2016/11/01
PAR
|
SE/H/0918/004_PAR
Date of last change:2016/11/01
Final PL
|
SE/H/0918/004_Final PL
Date of last change:2016/05/17
Final SPC
|
SE/H/0918/004_Final SPC
Date of last change:2016/05/17
市场状态
Positive
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