This brand name is authorized in Finland
The drug DITEKIPOL contains a combination of these active pharmaceutical ingredients (APIs):
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1
Clostridium tetani toxoid, adsorbed
UNII K3W1N8YP13 - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
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2
Corynebacterium diphtheriae toxoid, adsorbed
UNII 3U7E3O07S8 - CORYNEBACTERIUM DIPHTHERIAE
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| 3 Bordetella pertussis toxoid, adsorbed |
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4
Poliovirus type 1 (Brunhilde), inactivated
UNII 0LVY784C09 - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
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5
Poliovirus type 2 (MEF-1), inactivated
UNII 23JE9KDF4R - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
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6
Poliovirus type 3 (Saukett), inactivated
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 code | Group title | Classification |
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| 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) |
|---|---|---|
| Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 569913, 569921 |
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