This brand name is authorized in United States. It is also authorized in New Zealand.
The drug QUADRACEL contains a combination of these active pharmaceutical ingredients (APIs):
1
|
UNII
IRH51QN26H - CORYNEBACTERIUM DIPHTHERIAE TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
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2
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UNII
K3W1N8YP13 - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
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3
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UNII
F4TN0IPY37 - BORDETELLA PERTUSSIS TOXOID ANTIGEN (GLUTARALDEHYDE INACTIVATED)
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4
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UNII
8C367IY4EY - BORDETELLA PERTUSSIS FILAMENTOUS HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)
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5
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UNII
63GD90PP8X - BORDETELLA PERTUSSIS PERTACTIN ANTIGEN
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6
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UNII
1O0600285A - BORDETELLA PERTUSSIS FIMBRIAE 2/3 ANTIGEN
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7
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UNII
0LVY784C09 - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
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8
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UNII
23JE9KDF4R - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
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9
|
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 | |
|---|---|---|
| J07CA02 | Diphtheria-pertussis-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) |
|---|---|---|
| NZ | Medicines and Medical Devices Safety Authority | 9814 |
| US | FDA, National Drug Code | 49281-562, 49281-564 |
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