This brand name is authorized in Australia, Austria, Brazil, Canada, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Japan, Lithuania, Netherlands, Nigeria, Poland, Romania, Singapore, South Africa, Spain, Turkey, UK.
The drug JEVTANA contains one active pharmaceutical ingredient (API):
1
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UNII
51F690397J - CABAZITAXEL
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Cabazitaxel is an antineoplastic agent that acts by disrupting the microtubular network in cells. Cabazitaxel binds to tubulin and promotes the assembly of tubulin into microtubules while simultaneously inhibiting their disassembly. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| JEVTANA Concentrate and solvent for solution for infusion | 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 | |
|---|---|---|
| L01CD04 | Cabazitaxel | L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01C Plant alkaloids and other natural products → L01CD Taxanes |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 4376H, 7236W |
| BR | Câmara de Regulação do Mercado de Medicamentos | 576720050064517 |
| CA | Health Products and Food Branch | 02369524 |
| EE | Ravimiamet | 1523719 |
| ES | Centro de información online de medicamentos de la AEMPS | 11676001, 11676001IP |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 483519 |
| FR | Base de données publique des médicaments | 64883869 |
| GB | Medicines & Healthcare Products Regulatory Agency | 191781, 383754 |
| HK | Department of Health Drug Office | 61193 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 6712 |
| JP | 医薬品医療機器総合機構 | 4240410A1020 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1059847 |
| NG | Registered Drug Product Database | A4-100070 |
| NL | Z-Index G-Standaard, PRK | 98434 |
| PL | Rejestru Produktów Leczniczych | 100243076 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W69352001 |
| SG | Health Sciences Authority | 14043P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699809760707 |
| ZA | Health Products Regulatory Authority | 45/26/0511 |
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