INFANRIX

This brand name is authorized in Lithuania, New Zealand, Poland, United States

Active ingredients

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

1 Tetanus toxoid
UNII K3W1N8YP13 - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Tetanus toxoid
2 Diphtheria toxoid
UNII IRH51QN26H - CORYNEBACTERIUM DIPHTHERIAE TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Diphtheria toxoid
3 Pertussis, purified antigen
UNII QSN5XO8ZSU - BORDETELLA PERTUSSIS TOXOID ANTIGEN (FORMALDEHYDE, GLUTARALDEHYDE INACTIVATED)
Read about Pertussis, purified antigen
4 Pertussis filamentous hemagglutinin
UNII 8C367IY4EY - BORDETELLA PERTUSSIS FILAMENTOUS HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Pertussis filamentous hemagglutinin
5 Pertussis, purified antigen
UNII I05O535NV6 - BORDETELLA PERTUSSIS PERTACTIN ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Pertussis, purified antigen

Medicine classification

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

ATC code Group title Classification
J07AJ52 Pertussis, purified antigen, combinations with toxoids J Antiinfectives for systemic use → J07 Vaccines → J07A Bacterial vaccines → J07AJ Pertussis vaccines
Discover more medicines within J07AJ52

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1007549
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 7344
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100224363
Country: US FDA, National Drug Code Identifier(s): 50090-2883, 58160-810

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