This brand name is authorized in Austria, Canada, Croatia, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Japan, Lithuania, Netherlands, New Zealand, Poland, Spain.
The drug SHINGRIX contains one active pharmaceutical ingredient (API):
1
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UNII
COB9FF6I46 - RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN
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Human varicella zoster immunoglobulin contains mainly immunoglobulin G (IgG) with a specifically high content of antibodies against varicella-zoster virus. It is used for prophylaxis against varicella zoster virus (VZV) infection. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| SHINGRIX Powder for suspension for injection | MPI, EU: SmPC | European Medicines Agency (EU) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07BK03 | 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) |
|---|---|---|
| CA | Health Products and Food Branch | 02468425 |
| EE | Ravimiamet | 1767315, 1767326 |
| ES | Centro de información online de medicamentos de la AEMPS | 1181272001 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 176947 |
| FR | Base de données publique des médicaments | 62887096 |
| HK | Department of Health Drug Office | 66840 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 9249 |
| IT | Agenzia del Farmaco | 046337010, 046337022 |
| JP | 医薬品医療機器総合機構 | 631341BE1028 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1085276, 1085277 |
| NL | Z-Index G-Standaard, PRK | 202843 |
| NZ | Medicines and Medical Devices Safety Authority | 20173 |
| PL | Rejestru Produktów Leczniczych | 100402280 |
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