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KABIVEN

INF EML 1X1540ML II

SÚKL code 0107100
Name of the product KABIVEN
_MA_MEDICATION_DETAIL_INFO_MED_NAME i KABIVEN
Supplement INF EML 1X1540ML II
Strenght
Pharmaceutical form Emulsion for infusion
Package 1X1540ML II
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)
GLUTAMIC ACID (ACIDUM GLUTAMICUM)
HISTIDINE (HISTIDINUM)
ISOLEUCINE (ISOLEUCINUM)
LEUCINE (LEUCINUM)
LYSINE HYDROCHLORIDE (LYSINI HYDROCHLORIDUM)
MAGNESIUM SULFATE HEPTAHYDRATE (MAGNESII SULFAS HEPTAHYDRICUS)
PHENYLALANINE (PHENYLALANINUM)
POTASSIUM CHLORIDE (KALII CHLORIDUM)
SODIUM ACETATE TRIHYDRATE (NATRII ACETAS TRIHYDRICUS)
SOYA-BEAN OIL, REFINED (SOJAE OLEUM RAFFINATUM)
THREONINE (THREONINUM)
TRYPTOPHAN (TRYPTOPHANUM)
TYROSINE (TYROSINUM)
VALINE (VALINUM)
METHIONINE (METHIONINUM)
PROLINE (PROLINUM)
SERINE (SERINUM)
GLUCOSE MONOHYDRATE (GLUCOSUM MONOHYDRICUM)
CALCIUM CHLORIDE DIHYDRATE (CALCII CHLORIDUM DIHYDRICUM)
SODIUM GLYCEROPHOSPHATE (NATRII GLYCEROPHOSPHAS)
ATC group B05BA10
ATC group name ROZTOKY PRO PARENTERÁLNÍ VÝŽIVU, KOMBINACE

Marketing authorisation information

Registration Number 76/ 199/01-C
Type of MA National
MA status R - active MA/authorised medicinal product
MA Holder Fresenius Kabi AB, Uppsala
MA Holder country ŠVÉDSKO

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