RAXONE

This brand name is authorized in Austria, Croatia, Estonia, Finland, France, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Romania, South Africa, UK.

Active ingredients

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

1	Idebenone UNII HB6PN45W4J - IDEBENONE
	Idebenone is an anti-oxidant assumed to be capable of transferring electrons directly to complex III of the mitochondrial electron transport chain, thereby restoring cellular energy (ATP) generation under experimental conditions of complex I deficiency. Similarly, in LHON idebenone can transfer electrons directly to complex III of the electron transport chain, thereby bypassing complex I which is affected by all three primary mtDNA mutations causing LHON, and restoring cellular ATP generation.
	Read more about Idebenone

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
RAXONE Film-coated tablet	MPI, EU: SmPC	European Medicines Agency (EU)

Medicine classification

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

ATC Group		Classification
N06BX13	Idebenone	N Nervous system → N06 Psychoanaleptics → N06B Psychostimulants, agents used for ADHD and nootropics → N06BX Other psychostimulants and nootropics
Discover more medicines within N06BX13

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	1697126
FI	Lääkealan turvallisuus- ja kehittämiskeskus	402673
FR	Base de données publique des médicaments	62612837
GB	Medicines & Healthcare Products Regulatory Agency	314618
IE	Health Products Regulatory Authority	88947
IL	מִשְׂרַד הַבְּרִיאוּת	8368
IT	Agenzia del Farmaco	044505016
LT	Valstybinė vaistų kontrolės tarnyba	1078066
NL	Z-Index G-Standaard, PRK	130710
PL	Rejestru Produktów Leczniczych	100354315
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W62508001
ZA	Health Products Regulatory Authority	52/1.6/0616