OPTIRAY

This brand name is authorized in Austria, Brazil, Canada, Ecuador, Spain, Finland, France, Hong Kong, Croatia, 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: HR	Agencija za lijekove i medicinske proizvode	Identifier(s): HR-H-719390136, HR-H-794402560, HR-H-975335989
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