This brand name is authorized in United States. It is also authorized in Brazil, Canada, Croatia, Cyprus, Ecuador, Estonia, Hong Kong SAR China, Lithuania, Malta, New Zealand, Poland, Romania, Singapore, Turkey.
The drug ADACEL contains a combination of these active pharmaceutical ingredients (APIs):
1
|
UNII
K3W1N8YP13 - CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
|
2
|
UNII
IRH51QN26H - CORYNEBACTERIUM DIPHTHERIAE TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
|
3
|
UNII
F4TN0IPY37 - BORDETELLA PERTUSSIS TOXOID ANTIGEN (GLUTARALDEHYDE INACTIVATED)
|
4
|
UNII
8C367IY4EY - BORDETELLA PERTUSSIS FILAMENTOUS HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)
|
5
|
UNII
63GD90PP8X - BORDETELLA PERTUSSIS PERTACTIN ANTIGEN
|
6
|
UNII
1O0600285A - BORDETELLA PERTUSSIS FIMBRIAE 2/3 ANTIGEN
|
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07AJ52 | Pertussis, purified antigen, combinations with toxoids | J Antiinfectives for systemic use → J07 Vaccines → J07A Bacterial vaccines → J07AJ Pertussis vaccines |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| BR | Câmara de Regulação do Mercado de Medicamentos | 576720060074617 |
| CA | Health Products and Food Branch | 02240255 |
| EE | Ravimiamet | 1428195, 1428207, 1428218, 1659405, 1659416 |
| HK | Department of Health Drug Office | 57327 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-373342184 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1038464, 1053396, 1073901, 1073902, 1080472, 1080473, 1080474, 1080475 |
| MT | Medicines Authority | MA573/01402 |
| NZ | Medicines and Medical Devices Safety Authority | 12359 |
| PL | Rejestru Produktów Leczniczych | 100368910 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W62830001, W62830002, W62830003, W62830004, W62830005, W62830006 |
| SG | Health Sciences Authority | 14232P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699625960466, 8699625960589 |
| US | FDA, National Drug Code | 49281-400 |
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