This brand name is authorized in United States. It is also authorized in Austria, Brazil, Canada, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Japan, Lithuania, Malta, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey, UK.
The drug VISIPAQUE contains one active pharmaceutical ingredient (API):
1
|
UNII
HW8W27HTXX - IODIXANOL
|
Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| VISIPAQUE Solution for injection | MPI, EU: SmPC | Medicines and Medical Devices Safety Authority (NZ) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| V08AB09 | Iodixanol | V Various → V08 Contrast media → V08A X-ray contrast media, iodinated → V08AB Watersoluble, nephrotropic, low osmolar X-ray contrast media |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| BR | Câmara de Regulação do Mercado de Medicamentos | 541612090001004, 541612090001114, 541612090001204, 541612090001704, 541612090001804, 541616070002203 |
| CA | Health Products and Food Branch | 02145766, 02145774 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 5005-MEE-0320 |
| EE | Ravimiamet | 1038114, 1038125, 1079344, 1079355, 1079366, 1079377, 1079388, 1079399, 1140905, 1140927, 1140972, 1140983, 1141029, 1141030, 1141074, 1141108, 1141153, 1141164, 1141175, 1141186 |
| ES | Centro de información online de medicamentos de la AEMPS | 60636, 60637 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 019121, 019132, 582882, 583401, 583450, 583518, 583609, 583708 |
| FR | Base de données publique des médicaments | 60567418, 60960777 |
| GB | Medicines & Healthcare Products Regulatory Agency | 377352, 398066, 398067, 80822, 80823, 80824, 80825, 80828 |
| HK | Department of Health Drug Office | 43490, 43491 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-289648429, HR-H-385628224 |
| JP | 医薬品医療機器総合機構 | 7219420A1031, 7219420A2038, 7219420A3034, 7219420A4030, 7219420A5037 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1010525, 1010526, 1010527, 1010528, 1011301, 1011302, 1011303, 1011304, 1021975, 1021976, 1021977, 1021979, 1021980, 1021981, 1026459, 1026460, 1069917, 1069918, 1069919, 1069920, 1078673, 1078674, 1078675, 1078676, 1078677, 1089024, 1089025, 1089026, 1089027 |
| MT | Medicines Authority | MA023/00201, MA023/00202 |
| NZ | Medicines and Medical Devices Safety Authority | 7154, 7159 |
| PL | Rejestru Produktów Leczniczych | 100093688, 100195147 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W12012001, W12012002, W12012003, W12012004, W12012005, W12012007, W12012008, W12013001, W12013002, W12013003, W12013004, W12013005, W12013006, W12013007 |
| SG | Health Sciences Authority | 08882P, 08883P |
| TN | Direction de la Pharmacie et du Médicament | 2453041, 2453042, 2453043 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699688772143, 8699688772150, 8699688772242, 8699688772259, 8699688772266 |
| US | FDA, National Drug Code | 0407-2222, 0407-2223 |
| ZA | Health Products Regulatory Authority | 31/28/0171, 31/28/0172, 31/28/0175, 31/28/0176, 31/28/0177, 36/28/0134, 36/28/0136 |
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