This brand name is authorized in Canada, United States
The drug CYSTO-CONRAY II contains one active pharmaceutical ingredient (API):
1
Iotalamic acid
UNII XUW72GOP7W - IOTHALAMATE MEGLUMINE
|
Iotalamic acid is intended for use as a diagnostic radiopaque medium. It is used in excretory urography, cerebral angiography, peripheral arteriography, venography, arthrography, direct cholangiography, endoscopic retrograde cholangiopancreatography, contrast enhancement of computed tomographic brain images, cranial computerized angiotomography, intravenous digital subtraction angiography and arterial digital subtraction angiography. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
CYSTO-CONRAY II Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/Old |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
V08AA04 | Iotalamic acid | V Various → V08 Contrast media → V08A X-ray contrast media, iodinated → V08AA Watersoluble, nephrotropic, high osmolar X-ray contrast media |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: CA | Health Products and Food Branch | Identifier(s): 00397466 |
Country: US | FDA, National Drug Code | Identifier(s): 0019-0862 |
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