DITEKIPOL

This brand name is authorized in Finland.

Active ingredients

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

1
UNII K3W1N8YP13 - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
 
Read more about Tetanus toxoid
2
UNII 3U7E3O07S8 - CORYNEBACTERIUM DIPHTHERIAE
 
Read more about Diphtheria toxoid
3
 
Read more about Pertussis toxoid
4
UNII 0LVY784C09 - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
 
Read more about Poliomyelitis, serotype 1
5
UNII 23JE9KDF4R - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
 
Read more about Poliomyelitis, serotype 2
6
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
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)
FI Lääkealan turvallisuus- ja kehittämiskeskus 569913, 569921

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