CERVARIX

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

Active ingredients

The drug CERVARIX contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 6LTE2DNX63 - HUMAN PAPILLOMAVIRUS TYPE 16 L1 CAPSID PROTEIN ANTIGEN
 
Read more about L1 protein of human papillomavirus type 16
2
UNII J2D279PEM5 - HUMAN PAPILLOMAVIRUS TYPE 18 L1 CAPSID PROTEIN ANTIGEN
 
Read more about L1 protein of human papillomavirus type 18

Medicine classification

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

ATC Group Classification
J07BM02 Papillomavirus (human types 16, 18) J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BM Papillomavirus vaccines
Discover more medicines within J07BM02

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 510611010150311
CA Health Products and Food Branch 02342227
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 28467-05-08
EE Ravimiamet 1312030, 1312041, 1312052, 1312063, 1312074, 1402906, 1402917, 1402928
ES Centro de información online de medicamentos de la AEMPS 07419004, 07419004IP, 07419006
FI Lääkealan turvallisuus- ja kehittämiskeskus 062507
FR Base de données publique des médicaments 64098181
HK Department of Health Drug Office 56180
JP 医薬品医療機器総合機構 631340QG1022
LT Valstybinė vaistų kontrolės tarnyba 1028303, 1028304, 1028305, 1028306, 1028307, 1028308, 1028309, 1028310, 1028311, 1036069, 1036070, 1036071
NG Registered Drug Product Database A6-0012
Switch country to Nigeria in order to find specific presentations of CERVARIX
NL Z-Index G-Standaard, PRK 81612
NZ Medicines and Medical Devices Safety Authority 12518
PL Rejestru Produktów Leczniczych 100178835
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W52318001, W52318002, W52318003, W52318004, W52318005
SG Health Sciences Authority 13374P
TN Direction de la Pharmacie et du Médicament 7063131
TR İlaç ve Tıbbi Cihaz Kurumu 8699522967544
ZA Health Products Regulatory Authority 41/30.1/0366

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