This brand name is authorized in Austria, Brazil, Croatia, Finland, France, Hong Kong SAR China, Ireland, Japan, New Zealand, Poland, Romania, Spain, Turkey, UK.
The drug IOMERON contains one active pharmaceutical ingredient (API):
1
|
UNII
17E17JBP8L - IOMEPROL
|
Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| IOMERON Solution for injection | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| V08AB10 | Iomeprol | 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 | 540715080002302, 540715080002402, 540715080002502, 540715080002602, 540715080002702, 540715080002802, 540715080002902 |
| ES | Centro de información online de medicamentos de la AEMPS | 60808, 60809, 60810, 60811 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 036355, 049040, 057714, 059975, 108200, 116634, 125061, 136154, 166270, 176028, 378690, 413354, 424385, 448171, 462664, 468944, 486093, 499928, 519367, 524068, 532800, 555637, 581036, 582660, 585673 |
| FR | Base de données publique des médicaments | 60495132, 63392333, 63625015, 64747367, 68543173 |
| GB | Medicines & Healthcare Products Regulatory Agency | 399373, 399384, 399386, 399389, 399399, 399401, 399403, 399414, 399416 |
| HK | Department of Health Drug Office | 42876, 42877, 42878, 42879 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-034202133, HR-H-414078129, HR-H-853568028 |
| JP | 医薬品医療機器総合機構 | 7219417A1030, 7219417A2036, 7219417A3032, 7219417A4039, 7219417A5035, 7219417A6031, 7219417A8034, 7219417A9030, 7219417G1032, 7219417G2039, 7219417G3035, 7219417G4031, 7219417G5038, 7219417G6034, 7219417G7030 |
| NZ | Medicines and Medical Devices Safety Authority | 7009, 7010, 7011 |
| PL | Rejestru Produktów Leczniczych | 100080190, 100080208, 100080214, 100080220, 100080237 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W43269001, W43269002, W43269003, W43269004, W43269005, W43270001, W43270002, W43270003, W43270004, W43271001, W43271002, W43271003, W43271004 |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699564772953, 8699564772960, 8699564772977, 8699564772984, 8699564772991, 8699564773011, 8699564773028, 8699564773035, 8699564773042, 8699564773059, 8699564773066, 8699564773073, 8699564773080, 8699564773097, 8699564773110, 8699564773127, 8699564773134, 8699564773141, 8699564773196 |
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