This brand name is authorized in Austria, France, Ireland, Malta, Netherlands, UK.
The drug REVAXIS contains a combination of these active pharmaceutical ingredients (APIs):
1
|
UNII
3U7E3O07S8 - CORYNEBACTERIUM DIPHTHERIAE
|
2
|
UNII
K3W1N8YP13 - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
|
3
|
UNII
0LVY784C09 - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
|
4
|
UNII
23JE9KDF4R - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
|
5
|
UNII
459ROM8M9M - POLIOVIRUS TYPE 3 ANTIGEN (FORMALDEHYDE INACTIVATED)
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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 |
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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