欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0918/002
药品名称
Numeta G16E
活性成分
Alanine 4.66 g
Arginine 4.89 g
Aspartic acid 3.5 g
Calcium chloride 2.06 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 monohydrate 7.2 g
Magnesium acetate 1.51 g
Methionine 1.4 g
OLIVE OIL 0.0 g
Ornithine hydrochloride 1.85 g
Phenylalanine 2.45 g
Potassium acetate 5.05 g
Proline 1.75 g
Serine 2.33 g
Sodium chloride 1.37 g
Sodium glycerophosphate 4.43 g
SOYBEAN OIL 0.0 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)
Numeta G16E
互认成员国 - 产品名称
Germany (DE)
NUMETA Ped G 16% E Emulsion zur Infusion
Denmark (DK)
Numeta Ped G16%E
Belgium (BE)
Numetzah G16%E émulsion pour perfusion
Netherlands (NL)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Numeta G 16 % E Emulsion zur Infusion
France (FR)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Norway (NO)
Czechia (CZ)
NUMETA Ped G16%E, Emulsion for infusion
Finland (FI)
Poland (PL)
NUMETA G16% E
许可日期
2010/12/15
最近更新日期
2024/10/23
药物ATC编码
B05BA10 combinations
申请类型
TypeLevel1:
Known Active Substance
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
Final PL
|
SE_H_0918_002_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0918_002_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_0918_002_PAR
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase