REVAXIS

This brand name is authorized in Austria, France, Ireland, Malta, Netherlands, UK.

Active ingredients

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

1
UNII 3U7E3O07S8 - CORYNEBACTERIUM DIPHTHERIAE
 
Read more about Diphtheria toxoid
2
UNII K3W1N8YP13 - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
 
Read more about Tetanus toxoid
3
UNII 0LVY784C09 - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
 
Read more about Poliomyelitis, serotype 1
4
UNII 23JE9KDF4R - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
 
Read more about Poliomyelitis, serotype 2
5
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
J07CA01 Diphtheria-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 J07CA01

Authorization and marketing

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

Country Identification scheme Identifier(s)
FR Base de données publique des médicaments 60917345
GB Medicines & Healthcare Products Regulatory Agency 73745
MT Medicines Authority AA1438/05501, AA1438/05502, AA565/37901, AA573/01901
NL Z-Index G-Standaard 14818434
NL Z-Index G-Standaard, PRK 67830

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