ULTRAVIST

This brand name is authorized in Austria, Brazil, Canada, Cyprus, Ecuador, Estonia, Spain, France, Hong Kong, Croatia, Israel, Lithuania, Malta, Nigeria, New Zealand, Poland, Romania, Singapore, Tunisia, Turkey, United States, South Africa

Active ingredients

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

1 Iopromide UNII 712BAC33MZ - IOPROMIDE

The contrast-giving substance in the iopromide formulations is iopromide, a non-ionic water-soluble derivative of triiodinated isophthalic acid in which the firmly bound iodine absorbs the X-rays. Injection of iopromide opacifies those vessels or body cavities in the path of flow of the contrast agent, permitting radio-graphic visualization of the internal structures until significant dilution occurs. Read about Iopromide

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
ULTRAVIST Solution for injection	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
V08AB05	Iopromide	V Various → V08 Contrast media → V08A X-ray contrast media, iodinated → V08AB Watersoluble, nephrotropic, low osmolar X-ray contrast media
Discover more medicines within V08AB05

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): 538912120020014, 538912120020114, 538912120020214, 538912120020314, 538912120020414, 538912120020514, 538912120020614, 538912120020714, 538919060028903, 538921030033303
Country: CA	Health Products and Food Branch	Identifier(s): 02078600, 02078619
Country: EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	Identifier(s): 28966-08-09, 29009-09-09
Country: EE	Ravimiamet	Identifier(s): 1004803, 1004836, 1079221, 1079232, 1079243, 1079254, 1079265, 1079276, 1079287, 1079298, 1079300, 1124794, 1398753
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 59611, 59613, 59614
Country: FR	Base de données publique des médicaments	Identifier(s): 60385522, 62729413, 65027575, 68373358
Country: HK	Department of Health Drug Office	Identifier(s): 43948, 43949
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 7005
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1007952, 1007954, 1010744, 1014624, 1014625, 1014626, 1021162, 1021163, 1021164, 1053346, 1066719, 1066720, 1066721, 1066722, 1066723, 1066724, 1066725, 1066726, 1066727, 1066728, 1066729, 1066730, 1066731, 1070871, 1070872, 1071142, 1071143, 1073644, 1073645, 1074968, 1074969, 1074970, 1074971, 1076337, 1076338, 1076339, 1076340, 1076341, 1076342, 1080786, 1080787, 1086431, 1086432, 1086433, 1086434
Country: MT	Medicines Authority	Identifier(s): MA1354/00401
Country: NG	Registered Drug Product Database	Identifier(s): 04-6502
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 5122, 5123, 8930
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100068779, 100068785
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W64051001, W64051002, W64051003, W64051004, W64051005, W64051006, W64052001, W64052002, W64052003, W64052004
Country: SG	Health Sciences Authority	Identifier(s): 05841P, 05845P
Country: TN	Direction de la Pharmacie et du Médicament	Identifier(s): 12853011, 12853012, 12853013, 12853014, 12853015
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8699546770014, 8699546770359, 8699546771936, 8699546773701, 8699546773718, 8699546773886, 8699546774142
Country: US	FDA, National Drug Code	Identifier(s): 50419-342, 50419-344, 50419-346
Country: ZA	Health Products Regulatory Authority	Identifier(s): 28/28/0642, 28/28/0643, 33/28/0082, 33/28/0083, 33/28/0084, 36/28/0137, 46/28/0109, 46/28/0110, V/28/173, V/28/174, V/28/175, V/28/176, V/28/177, V/28/178, V/28/179