This brand name is authorized in Austria, Australia, Brazil, Canada, Cyprus, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Japan, Lithuania, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, Tunisia, Turkey, United Kingdom, United States, South Africa
The drug VOTRIENT contains one active pharmaceutical ingredient (API):
1
Pazopanib
UNII 33Y9ANM545 - PAZOPANIB HYDROCHLORIDE
|
Pazopanib is an orally administered, potent multi-target tyrosine kinase inhibitor (TKI) of vascular endothelial growth factor receptors (VEGFR) -1, -2, and -3, platelet-derived growth factor (PDGFR) -α and -β, and stem cell factor receptor (c-KIT), with IC50 values of 10, 30, 47, 71, 84 and 74 nM, respectively. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
VOTRIENT Film-coated tablets | European Medicines Agency (EU) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
L01EX03 | Pazopanib | L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01E Protein kinase inhibitors → L01EX Other protein kinase inhibitors |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: AU | Pharmaceutical Benefits Scheme | Identifier(s): 10041L, 10042M, 10043N, 10047T, 10052C, 10054E, 11252F, 11261Q, 2029T, 2030W, 2201W, 2232L |
Country: BR | Câmara de Regulação do Mercado de Medicamentos | Identifier(s): 526517050089517, 526517050089617, 526517050089717 |
Country: CA | Health Products and Food Branch | Identifier(s): 02352303 |
Country: EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | Identifier(s): 2776-MEE-0517 |
Country: EE | Ravimiamet | Identifier(s): 1482027, 1482038, 1482049, 1482050 |
Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 10628001, 10628004 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 058261, 085366 |
Country: FR | Base de données publique des médicaments | Identifier(s): 62894653, 63803884 |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 174621, 174624 |
Country: HK | Department of Health Drug Office | Identifier(s): 60351, 60352, 62096, 62097 |
Country: IE | Health Products Regulatory Authority | Identifier(s): 88558, 88559 |
Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 6703, 6705 |
Country: IT | Agenzia del Farmaco | Identifier(s): 039945011, 039945023, 039945035, 039945047 |
Country: JP | 医薬品医療機器総合機構 | Identifier(s): 4291028F1023 |
Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1055472, 1055473, 1055474, 1055475 |
Country: MX | Comisión Federal para la Protección contra Riesgos Sanitarios | Identifier(s): 174M2011 |
Country: NL | Z-Index G-Standaard, PRK | Identifier(s): 95265, 95273 |
Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 13984, 13985 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100222878, 100222884 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W64502001, W64502002, W64503001, W64503002 |
Country: SG | Health Sciences Authority | Identifier(s): 14022P, 14023P |
Country: TN | Direction de la Pharmacie et du Médicament | Identifier(s): 1243091, 1243092 |
Country: TR | İlaç ve Tıbbi Cihaz Kurumu | Identifier(s): 8699504092134, 8699504092141, 8699504092158, 8699504092165 |
Country: US | FDA, National Drug Code | Identifier(s): 0078-0670 |
Country: ZA | Health Products Regulatory Authority | Identifier(s): 44/26/0348, 44/26/0349 |
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