NOZINAN

This brand name is authorized in Austria, Canada, Croatia, Estonia, France, Ireland, Malta, Netherlands, New Zealand, Tunisia, UK.

Active ingredients

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

1
UNII 5KN5Y9V01K - LEVOMEPROMAZINE MALEATE
 

Levomepromazine resembles chlorpromazine and promethazine in the pattern of its pharmacology. It possesses anti-emetic, antihistamine and anti-adrenaline activity and exhibits a strong sedative effect.

 
Read more about Levomepromazine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 NOZINAN Tablets MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)
 NOZINAN Solution for injection / infusion MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group Classification
N05AA02 Levomepromazine N Nervous system → N05 Psycholeptics → N05A Antipsychotics → N05AA Phenothiazines with aliphatic side-chain
Discover more medicines within N05AA02

Authorization and marketing

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

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 01927698
EE Ravimiamet 1882122
FR Base de données publique des médicaments 60548802, 60669978, 63148279, 64026417, 67348996, 67477165, 68270422, 69074348, 69192161
GB Medicines & Healthcare Products Regulatory Agency 162146, 25940, 373997, 376962, 381567, 41831
HR Agencija za lijekove i medicinske proizvode HR-H-260996650, HR-H-983495354
IE Health Products Regulatory Authority 36501
MT Medicines Authority AA565/22303
NL Z-Index G-Standaard 12824119
NL Z-Index G-Standaard, PRK 2097, 6580
NZ Medicines and Medical Devices Safety Authority 21069, 21070, 713, 714, 715
TN Direction de la Pharmacie et du Médicament 6390091, 6390092

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