NUMETA G16%E

INF EML 1X500ML

SÚKL code 0202092
Name of the product NUMETA G16%E
_MA_MEDICATION_DETAIL_INFO_MED_NAME i NUMETA G16%E
Supplement INF EML 1X500ML
Strenght
Pharmaceutical form Emulsion for infusion
Package 1X500ML
Route Intravenous use
Language of the pack Czech
Wrap type Bag
Legal status na lékařský předpis
Active substance ALANINE (ALANINUM)
GLYCINE (GLYCINUM)
ARGININE (ARGININUM)
ASPARTIC ACID (ACIDUM ASPARTICUM)
CYSTEINE (CYSTEINUM)
GLUTAMIC ACID (ACIDUM GLUTAMICUM)
HISTIDINE (HISTIDINUM)
ISOLEUCINE (ISOLEUCINUM)
LEUCINE (LEUCINUM)
PHENYLALANINE (PHENYLALANINUM)
POTASSIUM ACETATE (KALII ACETAS)
SODIUM CHLORIDE (NATRII CHLORIDUM)
SOYA-BEAN OIL, REFINED (SOJAE OLEUM RAFFINATUM)
TAURINE (TAURINUM)
THREONINE (THREONINUM)
TRYPTOPHAN (TRYPTOPHANUM)
TYROSINE (TYROSINUM)
VALINE (VALINUM)
METHIONINE (METHIONINUM)
PROLINE (PROLINUM)
MAGNESIUM ACETATE TETRAHYDRATE (MAGNESII ACETAS TETRAHYDRICUS)
SERINE (SERINUM)
ORNITHINE HYDROCHLORIDE (ORNITHINI HYDROCHLORIDUM)
GLUCOSE MONOHYDRATE (GLUCOSUM MONOHYDRICUM)
CALCIUM CHLORIDE DIHYDRATE (CALCII CHLORIDUM DIHYDRICUM)
LYSINE MONOHYDRATE (LYSINUM MONOHYDRICUM)
OLIVE OIL, REFINED (OLIVAE OLEUM RAFFINATUM)
SODIUM GLYCEROPHOSPHATE, HYDRATE (NATRII GLYCEROPHOSPHAS HYDRICUS)
ATC group B05BA10
ATC group name ROZTOKY PRO PARENTERÁLNÍ VÝŽIVU, KOMBINACE

Marketing authorisation information

Registration Number 76/ 329/11-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state
MA status R - active MA/authorised medicinal product
MA Holder BAXTER CZECH spol. s r.o., Praha
MA Holder country ČESKÁ REPUBLIKA

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