This brand name is authorized in United States. It is also authorized in Austria, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Lithuania, Malta, New Zealand, Poland, Romania, Singapore, Spain, Turkey, UK.
The drug VARIVAX contains one active pharmaceutical ingredient (API):
1
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UNII
GPV39ZGD8C - VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN
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Natural infection induces a cellular and humoral immune response to the varicella-zoster virus, which can be rapidly detected following infection. IgG, IgM and IgA directed against viral proteins usually appear at the same time that a cellular immune response can be demonstrated, making the relative contribution of humoral and cellular immunity to disease progression difficult to ascertain. Vaccination has been shown to induce both humoral and cell-mediated types of immunity. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07BK01 | Varicella, live attenuated | J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BK Varicella zoster vaccines |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 79-MBE-1216 |
| EE | Ravimiamet | 1182372, 1182383 |
| ES | Centro de información online de medicamentos de la AEMPS | 65709 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 576856 |
| FR | Base de données publique des médicaments | 69201849 |
| GB | Medicines & Healthcare Products Regulatory Agency | 79956 |
| HK | Department of Health Drug Office | 39958 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-920622763 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1019610, 1019611, 1019612, 1019613, 1019614, 1019615 |
| MT | Medicines Authority | MA224/00501 |
| NZ | Medicines and Medical Devices Safety Authority | 8159 |
| PL | Rejestru Produktów Leczniczych | 100420673 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W66309003, W66309004, W66309005, W66309006 |
| SG | Health Sciences Authority | 13090P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699636950159 |
| US | FDA, National Drug Code | 0006-4826, 0006-4827 |
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