This brand name is authorized in Canada, Croatia, Estonia, Finland, France, Hong Kong SAR China, Israel, Japan, Lithuania, Malta, Poland, Singapore, South Africa, Tunisia.
The drug IMOVAX POLIO contains a combination of these active pharmaceutical ingredients (APIs):
1
|
UNII
0LVY784C09 - POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED)
|
2
|
UNII
23JE9KDF4R - POLIOVIRUS TYPE 2 ANTIGEN (FORMALDEHYDE INACTIVATED)
|
3
|
UNII
459ROM8M9M - POLIOVIRUS TYPE 3 ANTIGEN (FORMALDEHYDE INACTIVATED)
|
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07BF03 | Poliomyelitis, trivalent, inactivated, whole virus | J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BF Poliomyelitis vaccines |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| CA | Health Products and Food Branch | 01959042 |
| EE | Ravimiamet | 1025985 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 000502 |
| FR | Base de données publique des médicaments | 63513354 |
| HK | Department of Health Drug Office | 06083 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-527075219 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 7532 |
| JP | 医薬品医療機器総合機構 | 631340UG1024 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1035087, 1035088, 1035089, 1035090 |
| MT | Medicines Authority | MA573/00901, MA573/00902 |
| PL | Rejestru Produktów Leczniczych | 100196626 |
| SG | Health Sciences Authority | 10608P |
| TN | Direction de la Pharmacie et du Médicament | 12063081 |
| ZA | Health Products Regulatory Authority | A38/30.1/0717 |
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