UROGRAFIN

This brand name is authorized in Estonia, Spain, Ireland, Japan, Lithuania, New Zealand

Active ingredients

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

1 Diatrizoic acid
UNII 5UVC90J1LK - DIATRIZOIC ACID
Read about Diatrizoic acid

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
UROGRAFIN Solution for 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
V08AA01 Diatrizoic acid V Various → V08 Contrast media → V08A X-ray contrast media, iodinated → V08AA Watersoluble, nephrotropic, high osmolar X-ray contrast media
Discover more medicines within V08AA01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1079412
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 23817
Country: JP 医薬品医療機器総合機構 Identifier(s): 7214400A2034, 7214400A5041, 7214400A6030
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1010502, 1010503, 1031777, 1091061
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 711, 712

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