REPEVAX

This brand name is authorized in Austria, France, Ireland, Malta, United Kingdom

Active ingredients

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

1 Diphtheria toxoid adsorbed
UNII 3U7E3O07S8 - CORYNEBACTERIUM DIPHTHERIAE
Read about Diphtheria toxoid
2 Tetanus toxoid adsorbed
UNII K3W1N8YP13 - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Tetanus toxoid
3 Purified pertussis toxoid (PT XD)
Read about Pertussis toxoid
4 Adsorbed purified filamentous hemagglutinin (FHA)
UNII 8C367IY4EY - BORDETELLA PERTUSSIS FILAMENTOUS HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Pertussis filamentous hemagglutinin
5 Pertussis toxoid
Read about Pertussis toxoid
6 Adsorbed purified pertactin (PRN)
UNII 2QNL82089R - BORDETELLA PERTUSSIS
Read about Pertactin
7 Inactivated poliovirus vaccine type I
UNII 0LVY784C09 - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Poliomyelitis, serotype 1
8 Inactivated poliovirus vaccine type II
UNII 23JE9KDF4R - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Poliomyelitis, serotype 2
9 Inactivated poliovirus vaccine type III
UNII 459ROM8M9M - POLIOVIRUS TYPE 3 ANTIGEN (FORMALDEHYDE INACTIVATED)
Read about Poliomyelitis, serotype 3
10 Adsorbed purified fimbrial Agglutinogens 2+3 (FIM)
UNII F92V3S521O - ALUMINUM PHOSPHATE
Read about Aluminium phosphate

Medicine classification

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

ATC code Group title 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)
Country: FR Base de données publique des médicaments Identifier(s): 67619892
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 88827
Country: MT Medicines Authority Identifier(s): AA770/09601, AA770/09602

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