KABIVEN PERIPHERAL
INF EML 4X1920ML II
SÚKL code | 0107122 |
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Name of the product | KABIVEN PERIPHERAL |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | KABIVEN PERIPHERAL |
Supplement | INF EML 4X1920ML II |
Strenght | |
Pharmaceutical form | Emulsion for infusion |
Package | 4X1920ML 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/ 200/01-C |
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Type of MA | National |
MA status | R - active MA/authorised medicinal product |
MA Holder | Fresenius Kabi AB, Uppsala |
MA Holder country | ŠVÉDSKO |