ESMERON

This brand name is authorized in Austria, Brazil, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Lithuania, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey, UK.

Active ingredients

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

1
UNII I65MW4OFHZ - ROCURONIUM BROMIDE
 

Rocuronium is a fast onset, intermediate acting non-depolarising neuromuscular blocking agent, possessing all of the characteristic pharmacological actions of this class of medicinal products (curariform agents). It acts by competing for nicotinic cholinoceptors at the motor end-plate.

 
Read more about Rocuronium

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 ESMERON Solution for injection 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
M03AC09 Rocuronium bromide M Musculo-skeletal system → M03 Muscle relaxants → M03A Muscle relaxants, peripherally acting agents → M03AC Other quaternary ammonium compounds
Discover more medicines within M03AC09

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 527316010017803
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 23.874-1-06-11
EE Ravimiamet 1040218, 1074282, 1138687, 1294321
ES Centro de información online de medicamentos de la AEMPS 61141
FI Lääkealan turvallisuus- ja kehittämiskeskus 095879
FR Base de données publique des médicaments 68986795
GB Medicines & Healthcare Products Regulatory Agency 165869
HK Department of Health Drug Office 39066
IL מִשְׂרַד הַבְּרִיאוּת 6270
LT Valstybinė vaistų kontrolės tarnyba 1015685, 1026892, 1056348
MX Comisión Federal para la Protección contra Riesgos Sanitarios 235M96
NL Z-Index G-Standaard, PRK 46280
NZ Medicines and Medical Devices Safety Authority 7027
PL Rejestru Produktów Leczniczych 100083744, 100083810
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W63436001, W63436002, W63436003
SG Health Sciences Authority 09479P
TN Direction de la Pharmacie et du Médicament 70131511H
TR İlaç ve Tıbbi Cihaz Kurumu 8699636770016, 8699636770030
ZA Health Products Regulatory Authority 30/17.1/0192, 30/17.1/0193, 34/17.1/0174

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