This brand name is authorized in United States. It is also authorized in Australia, Austria, Brazil, Canada, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Italy, Japan, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey, UK.
The drug PEGASYS contains one active pharmaceutical ingredient (API):
1
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UNII
Q46947FE7K - PEGINTERFERON ALFA-2A
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Peginterferon alpha-2a is a pegylated interferon alfa-2a that possesses the in vitro antiviral and antiproliferative activities that are characteristic of interferon alfa-2a. Peginterferon alpha-2a is indicated for the treatment of hepatitis B and C. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| PEGASYS Solution 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 | |
|---|---|---|
| L03AB11 | Peginterferon alfa-2a | L Antineoplastic and immunomodulating agents → L03 Immunostimulants → L03A Immunostimulants → L03AB Interferons |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 11037X, 11416W, 6439X, 6449K, 9515T, 9516W |
| BR | Câmara de Regulação do Mercado de Medicamentos | 529204002151210 |
| CA | Health Products and Food Branch | 02248077 |
| EE | Ravimiamet | 1110340, 1110351, 1110362, 1110373, 1110384, 1110395, 1110407, 1110418, 1214828, 1214839, 1609523, 1609534, 1609545, 1609556, 1609567, 1609578, 1646197, 1820281, 1843905, 1847853, 1888274 |
| ES | Centro de información online de medicamentos de la AEMPS | 02221006, 02221008, 102221017 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 008767, 008782 |
| FR | Base de données publique des médicaments | 64347476, 67042907, 67134227 |
| GB | Medicines & Healthcare Products Regulatory Agency | 226859, 43381, 43384 |
| HK | Department of Health Drug Office | 51529, 51530 |
| IE | Health Products Regulatory Authority | 88365, 88402 |
| IT | Agenzia del Farmaco | 035683034, 035683046, 035683059, 035683061, 035683073, 035683085, 035683150 |
| JP | 医薬品医療機器総合機構 | 6399419A1022, 6399419A2029 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1004853, 1011191, 1011192, 1011193, 1011194, 1011195, 1030176, 1030177, 1030178, 1030179, 1064244, 1064245, 1064246, 1064247, 1064248, 1064249, 1071714 |
| NL | Z-Index G-Standaard | 14753588, 14753596 |
| NL | Z-Index G-Standaard, PRK | 105740, 106364, 106372, 63533, 63541 |
| NZ | Medicines and Medical Devices Safety Authority | 10133 |
| PL | Rejestru Produktów Leczniczych | 100112598, 100112606, 100112612, 100112629, 100295825 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W68070001, W68070002, W68070003 |
| SG | Health Sciences Authority | 12313P, 12314P |
| TN | Direction de la Pharmacie et du Médicament | 4773014H |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699514950004, 8699514950257, 8699514950264, 8699514950271 |
| US | FDA, National Drug Code | 0004-0350, 0004-0357 |
| ZA | Health Products Regulatory Authority | 38/26/0180 |
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