SLENYTO

This brand name is authorized in Austria, Estonia, Spain, Finland, France, Croatia, Ireland, Israel, Italy, Lithuania, New Zealand, Poland, United Kingdom

Active ingredients

The drug SLENYTO contains one active pharmaceutical ingredient (API):

1 Melatonin
UNII JL5DK93RCL - MELATONIN

Melatonin is a naturally occurring hormone produced by the pineal gland and is structurally related to serotonin. Physiologically, melatonin secretion increases soon after the onset of darkness, peaks at 2-4 am and diminishes during the second half of the night. Melatonin is associated with the control of circadian rhythms and entrainment to the light-dark cycle. It is also associated with a hypnotic effect and increased propensity for sleep.

Read about Melatonin

Medicine classification

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

ATC code Group title Classification
N05CH01 Melatonin N Nervous system → N05 Psycholeptics → N05C Hypnotics and sedatives → N05CH Melatonin receptor agonists
Discover more medicines within N05CH01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1780501, 1780512, 1813575
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1181318003, 1181318005
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 067311, 143985
Country: FR Base de données publique des médicaments Identifier(s): 64061763, 64322882
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 368009, 368012
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8813, 8814
Country: IT Agenzia del Farmaco Identifier(s): 047187012, 047187024, 047187036, 047187048, 047187051
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1086403, 1086405, 1087372
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 21661, 21662
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100411349, 100411355

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