This brand name is authorized in United States. It is also authorized in Australia, Austria, Brazil, Canada, Croatia, Cyprus, Estonia, France, Hong Kong SAR China, Ireland, Italy, Japan, Lithuania, Mexico, Netherlands, New Zealand, Poland, Romania, Spain, UK.
The drug RENAGEL contains one active pharmaceutical ingredient (API):
1
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UNII
GLS2PGI8QG - SEVELAMER HYDROCHLORIDE
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Sevelamer is a non-absorbed phosphate binding crosslinked polymer, free of metal and calcium. Sevelamer contains multiple amines separated by one carbon from the polymer backbone which become protonated in the stomach. These protonated amines bind negatively charged ions such as dietary phosphate in the intestine. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| V03AE02 | Sevelamer | V Various → V03 All other therapeutic products → V03A All other therapeutic products → V03AE Drugs for treatment of hyperkalemia and hyperphosphatemia |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 2142R, 9546K, 9620H |
| BR | Câmara de Regulação do Mercado de Medicamentos | 576720090086717 |
| CA | Health Products and Food Branch | 02244310 |
| EE | Ravimiamet | 1123063, 1123074, 1215155, 1215166, 1215177, 1215188, 1215199 |
| ES | Centro de información online de medicamentos de la AEMPS | 99123012 |
| FR | Base de données publique des médicaments | 68950692 |
| GB | Medicines & Healthcare Products Regulatory Agency | 182909, 368722, 375941, 381658 |
| HK | Department of Health Drug Office | 52216 |
| IT | Agenzia del Farmaco | 034676080 |
| JP | 医薬品医療機器総合機構 | 2190025F1036 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1030653, 1030654, 1030655, 1030656, 1030657, 1030658, 1030659, 1030660, 1050549 |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 001M2007 |
| NL | Z-Index G-Standaard, PRK | 60496 |
| NZ | Medicines and Medical Devices Safety Authority | 11629 |
| PL | Rejestru Produktów Leczniczych | 100111334, 100111340 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W08985002 |
| US | FDA, National Drug Code | 58468-0021 |
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