NDAINJECTIONINJECTABLE
Approved
Dec 1985
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
5
Data completeness
4/8 — Partial
ISOVUE-200 (iopamidol) by Bracco is x-ray contrast activity [moa]. Approved for radiographic contrast agent [epc]. First approved in 1985.
Drug data last refreshed 15h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
ISOVUE-200 (iopamidol) is a non-ionic radiographic contrast agent administered by injection for X-ray imaging procedures. It enhances visualization of internal structures during diagnostic radiography by increasing radiodensity. The drug works through X-ray contrast activity to improve image quality for clinical assessment.
LOE Approaching2.3 years to LOE
Product approaching loss of exclusivity with moderate competitive pressure (30/100), signaling potential team consolidation and transition planning activities.
Mechanism of Action
X-Ray Contrast Activity
Pharmacologic Class:
Radiographic Contrast Agent
Indications (1)
Clinical Trials (5)
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
Safety Study of GE-145 320 mg I/mL Injection vs. Iopamidol 370 mg I/mL in Elderly Subjects Undergoing Coronary Procedure
Started Nov 2010
284 enrolled
Chronic Renal InsufficiencyDiabete MellitusCongestive Heart Failure
Renal Safety of Iopamidol Versus Iodixanol During Coronary Angiography in Diabetic Patients
Started Mar 2009
23 enrolled
Chronic Renal ImpairmentDiabetes Mellitus
Coronary MDCTA With Iopamidol Injection 370
Started Nov 2007
210 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.