VOLULYTE

This brand name is authorized in Austria, Cyprus, Estonia, Finland, Hong Kong SAR China, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, Spain.

Active ingredients

The drug VOLULYTE contains a combination of these active pharmaceutical ingredients (APIs):

1	Poly (0-2-hydroxyethyl) starch (M.W 200000) UNII 1GVO236S58 - HYDROXYETHYL STARCH 130/0.4
	Read more about HAES
2	Sodium acetate trihydrate UNII 4550K0SC9B - SODIUM ACETATE
	Read more about Sodium acetate
3	Sodium chloride UNII 451W47IQ8X - SODIUM CHLORIDE
	Sodium chloride is the principle salt involved in maintaining the osmotic tension of blood and tissues. Changes in osmotic tension influence the movement of fluids and diffusion of salts in cellular tissue.
	Read more about Sodium chloride
4	Potassium chloride UNII 660YQ98I10 - POTASSIUM CHLORIDE
	Potassium plays a vital physiological role in maintenance of normal electrical excitability of nerve and muscle. It is also important in the genesis and correction of imbalances of acid-base metabolism.
	Read more about Potassium chloride
5	Magnesium chloride hexahydrate UNII 02F3473H9O - MAGNESIUM CHLORIDE
	Read more about Magnesium chloride

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group		Classification
B05AA07	Hydroxyethylstarch	B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05A Blood and related products → B05AA Blood substitutes and plasma protein fractions
Discover more medicines within B05AA07

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
EE	Ravimiamet	1223323, 1223334, 1223345, 1223356, 1223367, 1223378, 1223389, 1223390, 1325304, 1325315
ES	Centro de información online de medicamentos de la AEMPS	70228
FI	Lääkealan turvallisuus- ja kehittämiskeskus	155885
HK	Department of Health Drug Office	58087
LT	Valstybinė vaistų kontrolės tarnyba	1022178, 1022179, 1022180, 1022181, 1022182, 1022183, 1022184, 1022185, 1083696, 1083697, 1083698, 1083699, 1083700, 1083701, 1083702
NL	Z-Index G-Standaard, PRK	86665
NZ	Medicines and Medical Devices Safety Authority	15246
PL	Rejestru Produktów Leczniczych	100115540
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W54129003, W54129004, W54129005, W54129006, W54129007, W54129010, W54129011, W54129012, W54129013, W54129014, W54129015, W54129016, W54129017, W54129018, W54129019
SG	Health Sciences Authority	13893P