This brand name is authorized in United States. It is also authorized in Austria, Canada, Croatia, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Singapore, Spain, UK.
The drug IXIARO contains one active pharmaceutical ingredient (API):
1
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UNII
DZ854I04ZE - JAPANESE ENCEPHALITIS VIRUS STRAIN SA 14-14-2 ANTIGEN (FORMALDEHYDE INACTIVATED)
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Japanese encephalitis is a disease caused by the mosquito-borne Japanese encephalitis virus (JEV). Japanese Encephalitis Vaccine acts by inducing antibodies that neutralize live JEV. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| IXIARO Japanese Encephalitis Vaccine | MPI, US: SPL/PLR | FDA, National Drug Code (US) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07BA02 | Encephalitis, Japanese, inactivated, whole virus | J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BA Encephalitis 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 | 02333279 |
| EE | Ravimiamet | 1412761 |
| ES | Centro de información online de medicamentos de la AEMPS | 08501002 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 157068 |
| FR | Base de données publique des médicaments | 62816512 |
| GB | Medicines & Healthcare Products Regulatory Agency | 153995 |
| HK | Department of Health Drug Office | 63173 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 6921 |
| IT | Agenzia del Farmaco | 039220013, 039220025 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1037141, 1037142 |
| NL | Z-Index G-Standaard, PRK | 139718 |
| PL | Rejestru Produktów Leczniczych | 100231080 |
| SG | Health Sciences Authority | 14108P |
| US | FDA, National Drug Code | 42515-002, 62195-051 |
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