NDAINJECTIONINJECTABLE
Approved
Aug 1997
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
4
Data completeness
4/8 — Partial
VISIPAQUE 270 (iodixanol) by GE HealthCare is x-ray contrast activity [moa]. Approved for radiographic contrast agent [epc]. First approved in 1997.
Drug data last refreshed 3h ago · AI intelligence enriched 6d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
VISIPAQUE 270 (iodixanol) is an injectable radiographic contrast agent used to enhance X-ray imaging during diagnostic and interventional procedures. It is an osmotically balanced, non-ionic contrast medium that provides superior visualization of blood vessels and organ structures. The drug works by absorbing X-rays and creating contrast between tissues, enabling clear imaging for clinical decision-making.
LOE Approaching
Product is in late lifecycle stage with moderate competitive pressure (30%), signaling potential team consolidation and shift toward lifecycle management rather than growth expansion.
Mechanism of Action
X-Ray Contrast Activity
Pharmacologic Class:
Radiographic Contrast Agent
Indications (1)
Clinical Trials (4)
Comparing Patient Comfort and Safety Between Iodixanol and Iopamidol in Patients Undergoing Peripheral Arteriography
Started Oct 2011
255 enrolled
Drug Safety
Iodixanol Versus Iopamidol in Patients Undergoing Contrast-Enhanced Computed Tomographic Imaging of Abdomen/Pelvis
Started May 2011
304 enrolled
Patient Comfort and Safety
Renal Safety of Iopamidol Versus Iodixanol During Coronary Angiography in Diabetic Patients
Started Mar 2009
23 enrolled
Chronic Renal ImpairmentDiabetes Mellitus
Iodixanol in Multidetector-Row Computed Tomography-Coronary Angiography (MDCT-CA)
Started Jul 2005
50 enrolled
Coronary Artery Disease
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.