POLIORIX

This brand name is authorized in Estonia, Poland

Active ingredients

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

1 Inactivated poliovirus type 1 (Mahoney strain)
UNII 0LVY784C09 - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Poliomyelitis, serotype 1
2 Inactivated poliovirus type 2 (strain MEF-1)
UNII 23JE9KDF4R - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Poliomyelitis, serotype 2
3 Inactivated poliovirus type 3 (Saukett strain)
UNII 459ROM8M9M - POLIOVIRUS TYPE 3 ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Poliomyelitis, serotype 3

Medicine classification

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

ATC code Group title Classification
J07BF03 Poliomyelitis, trivalent, inactivated, whole virus J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BF Poliomyelitis vaccines
Discover more medicines within J07BF03

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1136012, 1136023, 1398506
Country: PL Rejestru Produktรณw Leczniczych Identifier(s): 100223375

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