OPTIRAY

This brand name is authorized in United States. It is also authorized in Austria, Brazil, Canada, Croatia, Ecuador, Finland, France, Hong Kong SAR China, Ireland, Japan, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Turkey, UK.

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 more about Ioversol

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
OPTIRAY Solution for injection or infusion	MPI, EU: SmPC	Health Products Regulatory Authority (IE)

Medicine classification

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

ATC Group		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)
BR	Câmara de Regulação do Mercado de Medicamentos	524500401151213, 524500402158211, 524500403154211, 524500405157216, 524500406153214, 524500407151215, 524500408156210, 524500414156219, 524500415152217, 524500416159215, 524500417155213, 524500418151211, 524501101151313, 524501201156317
CA	Health Products and Food Branch	01900854, 02035626
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	2254-MEE-0616, 2421-MEE-0916, 2489-MEE-0916
ES	Centro de información online de medicamentos de la AEMPS	58468, 58469, 60713, 60714, 62067, 62068, 62069, 62070
FI	Lääkealan turvallisuus- ja kehittämiskeskus	015942, 015993, 123409, 193441, 199430, 199471, 199513, 199638, 199919, 371203, 371286, 371856, 406629, 406736, 406777, 440172, 440321, 440826, 440867, 516888, 562194
FR	Base de données publique des médicaments	65772900, 67722465
GB	Medicines & Healthcare Products Regulatory Agency	325768, 325777, 325805, 325809, 325810, 392476, 79005, 79011, 79013, 79015, 79017, 79019, 79803, 79819, 79821, 79823, 79827, 79829, 80061, 80063, 80067
HK	Department of Health Drug Office	38525, 38526, 38527, 38528
HR	Agencija za lijekove i medicinske proizvode	HR-H-719390136, HR-H-794402560, HR-H-975335989
JP	医薬品医療機器総合機構	7219416A8030, 7219416A9036, 7219416G1038, 7219416G3030, 7219416G4037, 7219416G9039, 7219416H1033, 7219416H2030, 7219416H3036, 7219416H4032, 7219416P1020
NZ	Medicines and Medical Devices Safety Authority	15441, 15442, 5613, 5614, 5615, 5617, 5618
PL	Rejestru Produktów Leczniczych	100120149, 100120155, 100120161, 100120178
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	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
SG	Health Sciences Authority	07748P, 13550P, 13551P, 13552P
TR	İlaç ve Tıbbi Cihaz Kurumu	8697706952058
US	FDA, National Drug Code	0019-1323, 0019-1324, 0019-1332, 0019-1333
ZA	Health Products Regulatory Authority	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