IMOVANE

This brand name is authorized in Australia, Brazil, Canada, Estonia, Finland, France, Hong Kong SAR China, Israel, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Turkey.

Active ingredients

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

1	Zopiclone UNII 03A5ORL08Q - ZOPICLONE
	Zopiclone is a hypnotic agent belonging to the cyclopyrrolone class of psychotherapeutic agents. It rapidly initiates and sustains sleep without reduction of total REM sleep and with preservation of slow wave sleep. Negligible residual effects are seen the following morning. Its pharmacological properties include hypnotic, sedative, anxiolytic, anticonvulsant and muscle-relaxant actions.
	Read more about Zopiclone

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
IMOVANE Tablet	MPI, Generic	Health Products Regulatory Authority (ZA)

Medicine classification

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

ATC Group		Classification
N05CF01	Zopiclone	N Nervous system → N05 Psycholeptics → N05C Hypnotics and sedatives → N05CF Benzodiazepine related drugs
Discover more medicines within N05CF01

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
AU	Pharmaceutical Benefits Scheme	4522B
BR	Câmara de Regulação do Mercado de Medicamentos	502806201116315, 576720080085217
CA	Health Products and Food Branch	01926799, 02216167
EE	Ravimiamet	1068083, 1764480, 1767304, 1839506, 1846313, 1846324, 1846335, 1888465, 1888476
FI	Lääkealan turvallisuus- ja kehittämiskeskus	085852, 085860, 087304, 087312, 087320
FR	Base de données publique des médicaments	61435939, 68508795
HK	Department of Health Drug Office	31180
IL	מִשְׂרַד הַבְּרִיאוּת	3329, 9348
LT	Valstybinė vaistų kontrolės tarnyba	1014326, 1086398, 1092751, 1092752, 1092753
NL	Z-Index G-Standaard, PRK	24732
NZ	Medicines and Medical Devices Safety Authority	4471
PL	Rejestru Produktów Leczniczych	100000882, 100322634, 100335654, 100344481, 100345635, 100355250, 100357408, 100358773, 100367186, 100367447, 100367720, 100368435, 100416482, 100445868
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W64484001, W64484002
SG	Health Sciences Authority	05047P
TR	İlaç ve Tıbbi Cihaz Kurumu	8699586010231, 8699586010279
ZA	Health Products Regulatory Authority	T/2.2/0104