This brand name is authorized in Austria, Brazil, Canada, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Lithuania, Netherlands, New Zealand, Nigeria, Poland, Romania, Singapore, Spain, Tunisia, Turkey, UK.
The drug NIMENRIX contains a combination of these active pharmaceutical ingredients (APIs):
1
|
UNII
1I86B47NY4 - NEISSERIA MENINGITIDIS GROUP A CAPSULAR POLYSACCHARIDE ANTIGEN
|
2
|
UNII
837RU6905N - NEISSERIA MENINGITIDIS GROUP C CAPSULAR POLYSACCHARIDE ANTIGEN
|
3
|
UNII
9F8QQ6EER1 - NEISSERIA MENINGITIDIS GROUP W-135 CAPSULAR POLYSACCHARIDE ANTIGEN
|
4
|
UNII
CBZ4BH7TJ1 - NEISSERIA MENINGITIDIS GROUP Y CAPSULAR POLYSACCHARIDE ANTIGEN
|
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07AH08 | Meningococcus A,C,Y,W-135, tetravalent purified polysaccharides antigen conjugated | J Antiinfectives for systemic use → J07 Vaccines → J07A Bacterial vaccines → J07AH Meningococcal 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 | 552817060000217 |
| CA | Health Products and Food Branch | 02402904 |
| EE | Ravimiamet | 1567504, 1567526, 1567548, 1567559, 1567560 |
| ES | Centro de información online de medicamentos de la AEMPS | 12767003, 12767004 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 121444 |
| FR | Base de données publique des médicaments | 69241562 |
| GB | Medicines & Healthcare Products Regulatory Agency | 205179 |
| HK | Department of Health Drug Office | 62095 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 7327 |
| IT | Agenzia del Farmaco | 042040016, 042040028, 042040030, 042040042, 042040055, 042040067, 042040079, 042040081 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1066217, 1066218, 1066219, 1066220, 1089520 |
| NG | Registered Drug Product Database | A6-0259 |
| NL | Z-Index G-Standaard, PRK | 196150 |
| NZ | Medicines and Medical Devices Safety Authority | 16572 |
| PL | Rejestru Produktów Leczniczych | 100121210, 100410150, 100419664, 100421253 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W64765001 |
| SG | Health Sciences Authority | 14534P |
| TN | Direction de la Pharmacie et du Médicament | 8013141, 8063161 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8681308964144 |
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