This brand name is authorized in United States. It is also authorized in Austria, Brazil, Canada, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Malta, Netherlands, New Zealand, Poland, Singapore, Spain, Turkey, UK.
The drug VAQTA contains one active pharmaceutical ingredient (API):
1
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UNII
Q04Q922K9Q - HEPATITIS A VIRUS STRAIN CR 326F ANTIGEN (FORMALDEHYDE INACTIVATED)
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Inactivated virus of a strain which was originally derived by further serial passage of a proven attenuated strain. The virus is grown, harvested, highly purified, formalin inactivated, and then adsorbed onto amorphous aluminum hydroxyphosphate sulphate. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| VAQTA ADULT Suspension for injection | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) | |
| VAQTA PAEDIATRIC Suspension for injection | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07BC02 | Hepatitis A, inactivated, whole virus | J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BC Hepatitis 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 | 525502501151411, 525502502158411, 525513100016103 |
| CA | Health Products and Food Branch | 02229702 |
| EE | Ravimiamet | 1713237 |
| ES | Centro de información online de medicamentos de la AEMPS | 61601, 61602 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 144089, 144774, 145292, 145300 |
| FR | Base de données publique des médicaments | 62087670 |
| GB | Medicines & Healthcare Products Regulatory Agency | 217330, 30053 |
| HK | Department of Health Drug Office | 41649, 41651 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 4826 |
| MT | Medicines Authority | AA1438/00602 |
| NL | Z-Index G-Standaard, PRK | 62049, 96237 |
| NZ | Medicines and Medical Devices Safety Authority | 7513 |
| PL | Rejestru Produktów Leczniczych | 100198460, 100224682 |
| SG | Health Sciences Authority | 10007P, 13717P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699636961360, 8699636961377 |
| US | FDA, National Drug Code | 0006-4095, 0006-4096, 0006-4831, 0006-4841 |
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