IOMERON

This brand name is authorized in Austria, Brazil, Spain, Finland, France, Hong Kong, Croatia, Ireland, Japan, New Zealand, Poland, Romania, Turkey, United Kingdom

Active ingredients

The drug IOMERON contains one active pharmaceutical ingredient (API):

1 Iomeprol
UNII 17E17JBP8L - IOMEPROL
Read about Iomeprol

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
IOMERON Solution for injection Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
V08AB10 Iomeprol V Various → V08 Contrast media → V08A X-ray contrast media, iodinated → V08AB Watersoluble, nephrotropic, low osmolar X-ray contrast media
Discover more medicines within V08AB10

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 540715080002302, 540715080002402, 540715080002502, 540715080002602, 540715080002702, 540715080002802, 540715080002902
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 60808, 60809, 60810, 60811
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 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
Country: FR Base de données publique des médicaments Identifier(s): 60495132, 63392333, 63625015, 64747367, 68543173
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 399373, 399384, 399386, 399389, 399399, 399401, 399403, 399414, 399416
Country: HK Department of Health Drug Office Identifier(s): 42876, 42877, 42878, 42879
Country: JP 医薬品医療機器総合機構 Identifier(s): 7219417A1030, 7219417A2036, 7219417A3032, 7219417A4039, 7219417A5035, 7219417A6031, 7219417A8034, 7219417A9030, 7219417G1032, 7219417G2039, 7219417G3035, 7219417G4031, 7219417G5038, 7219417G6034, 7219417G7030
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 7009, 7010, 7011
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100080190, 100080208, 100080214, 100080220, 100080237
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W43269001, W43269002, W43269003, W43269004, W43269005, W43270001, W43270002, W43270003, W43270004, W43271001, W43271002, W43271003, W43271004
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699564772953, 8699564772960, 8699564772977, 8699564772984, 8699564772991, 8699564773011, 8699564773028, 8699564773035, 8699564773042, 8699564773059, 8699564773066, 8699564773073, 8699564773080, 8699564773097, 8699564773110, 8699564773127, 8699564773134, 8699564773141, 8699564773196

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