BOOSTRIX POLIO

This brand name is authorized in Finland, Hong Kong SAR China, Israel, Lithuania, Malta, Netherlands, Poland, Romania, Singapore, Spain, Turkey.

Active ingredients

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

`1`	Diphtheria toxoid UNII `3U7E3O07S8` - CORYNEBACTERIUM DIPHTHERIAE
	Read more about Diphtheria toxoid
`2`	Tetanus toxoid UNII `K3W1N8YP13` - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
	Read more about Tetanus toxoid
`3`	Pertussis toxoid
	Read more about Pertussis toxoid
`4`	Pertussis filamentous hemagglutinin UNII `8C367IY4EY` - BORDETELLA PERTUSSIS FILAMENTOUS HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)
	Read more about Pertussis filamentous hemagglutinin
`5`	Pertactin UNII `2QNL82089R` - BORDETELLA PERTUSSIS
	Read more about Pertactin
`6`	Poliomyelitis, serotype 1 UNII `0LVY784C09` - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
	Read more about Poliomyelitis, serotype 1
`7`	Poliomyelitis, serotype 2 UNII `23JE9KDF4R` - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
	Read more about Poliomyelitis, serotype 2
`8`	Poliomyelitis, serotype 3 UNII `459ROM8M9M` - POLIOVIRUS TYPE 3 ANTIGEN (FORMALDEHYDE INACTIVATED)
	Read more about Poliomyelitis, serotype 3

Medicine classification

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

ATC Group		Classification
J07CA02	Diphtheria-pertussis-poliomyelitis-tetanus	J Antiinfectives for systemic use → J07 Vaccines → J07C Bacterial and viral vaccines, combined → J07CA Bacterial and viral vaccines, combined
Discover more medicines within J07CA02

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
ES	Centro de información online de medicamentos de la AEMPS	66462
FI	Lääkealan turvallisuus- ja kehittämiskeskus	387208
HK	Department of Health Drug Office	55589
IL	מִשְׂרַד הַבְּרִיאוּת	7206
LT	Valstybinė vaistų kontrolės tarnyba	1076511, 1076512, 1076513, 1076514
MT	Medicines Authority	PI1438/02601A
NL	Z-Index G-Standaard	14983842
NL	Z-Index G-Standaard, PRK	86584
PL	Rejestru Produktów Leczniczych	100182297, 100182305
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W59173001, W59173002, W59173003, W59173004, W59173005, W59173006
SG	Health Sciences Authority	15888P
TR	İlaç ve Tıbbi Cihaz Kurumu	8699522967575

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