OPTIRAY

This brand name is authorized in Austria, Brazil, Canada, Ecuador, Spain, Finland, France, Hong Kong, Ireland, Japan, New Zealand, Poland, Romania, Singapore, Turkey, United Kingdom, United States, South Africa

Active ingredients

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

1 Ioversol
UNII N3RIB7X24K - IOVERSOL

Ioversol is a non-ionic X-ray contrast medium. Intravascular injection of ioversol opacifies those vessels in the path of the flow of the contrast medium, permitting radiographic visualisation of the internal structures until significant haemodilution occurs.

Read about Ioversol

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
OPTIRAY Solution for injection or infusion Health Products Regulatory Authority (IE) 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
V08AB07 Ioversol V Various → V08 Contrast media → V08A X-ray contrast media, iodinated → V08AB Watersoluble, nephrotropic, low osmolar X-ray contrast media
Discover more medicines within V08AB07

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): 524500401151213, 524500402158211, 524500403154211, 524500405157216, 524500406153214, 524500407151215, 524500408156210, 524500414156219, 524500415152217, 524500416159215, 524500417155213, 524500418151211, 524501101151313, 524501201156317
Country: CA Health Products and Food Branch Identifier(s): 01900854, 02035626
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 2254-MEE-0616, 2421-MEE-0916, 2489-MEE-0916
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 58468, 58469, 60713, 60714, 62067, 62068, 62069, 62070
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 015942, 015993, 123409, 193441, 199430, 199471, 199513, 199638, 199919, 371203, 371286, 371856, 406629, 406736, 406777, 440172, 440321, 440826, 440867, 516888, 562194
Country: FR Base de données publique des médicaments Identifier(s): 65772900, 67722465
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 325768, 325777, 325805, 325809, 325810, 392476, 79005, 79011, 79013, 79015, 79017, 79019, 79803, 79819, 79821, 79823, 79827, 79829, 80061, 80063, 80067
Country: HK Department of Health Drug Office Identifier(s): 38525, 38526, 38527, 38528
Country: JP 医薬品医療機器総合機構 Identifier(s): 7219416A8030, 7219416A9036, 7219416G1038, 7219416G3030, 7219416G4037, 7219416G9039, 7219416H1033, 7219416H2030, 7219416H3036, 7219416H4032, 7219416P1020
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 15441, 15442, 5613, 5614, 5615, 5617, 5618
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100120149, 100120155, 100120161, 100120178
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W63698001, W63698002, W63698003, W63698004, W63698005, W63698006, W63698007, W63698008, W63698009, W63698010, W63699001, W63699002, W63699003, W63699004, W63699005, W63699006, W63699007, W63699008, W63699009, W63699010, W63699011, W63699012, W63699013, W63699014, W63699015, W63699016, W63699017, W63699018, W63699019, W63699020, W63699021, W63699022, W63699023, W63699024, W63699025, W63700001, W63700002, W63700003, W63700004, W63700005, W63700006, W63700007, W63700008, W63700009, W63700010, W63700011, W63700012, W63700013, W63700014, W63700015, W63700016, W63700017, W63700018, W63701001, W63701002, W63701003, W63701004, W63701005, W63701006, W63701007, W63701008, W63701009, W63701010, W63701011, W63701012, W63701013, W63701014, W63701015, W63701016, W63701017, W63701018, W63701019, W63701020, W63701021, W63701022, W63701023, W63701024, W63701025, W63701026, W63701027, W63701028
Country: SG Health Sciences Authority Identifier(s): 07748P, 13550P, 13551P, 13552P
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8697706952058
Country: US FDA, National Drug Code Identifier(s): 0019-1323, 0019-1324, 0019-1332, 0019-1333
Country: ZA Health Products Regulatory Authority Identifier(s): 30/28/0281, 30/28/0282, 34/28/0099, 34/28/0100, 34/28/0101, A39/28/0614, A40/28/0245, A40/28/0246, Z/28/412, Z/28/414, Z/28/416, Z/28/417, Z/28/418, Z/28/419, Z/28/420, Z/28/421, Z/28/422

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.