This brand name is authorized in Croatia, Lithuania, Poland, Romania, Tunisia
The drug DULTAVAX contains a combination of these active pharmaceutical ingredients (APIs):
1
Diphtheria toxoid
UNII 3U7E3O07S8 - CORYNEBACTERIUM DIPHTHERIAE
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2
Tetanus toxoid
UNII K3W1N8YP13 - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
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3
Inactivated poliovirus type 1
UNII 0LVY784C09 - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
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4
Inactivated poliovirus type 2
UNII 23JE9KDF4R - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
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5
Inactivated poliovirus type 3
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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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) |
---|---|---|
Country: HR | Agencija za lijekove i medicinske proizvode | Identifier(s): HR-H-868511800 |
Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1011585, 1058338, 1058339 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100223406 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W42784001, W42784002, W42784004, W42784005, W42784007, W42784008, W42784009, W42784010 |
Country: TN | Direction de la Pharmacie et du Médicament | Identifier(s): 12063041 |
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