SUFLAVE
Peakpolyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution
NDAORALFOR SOLUTION
Approved
Jun 2023
Lifecycle
Peak
Competitive Pressure
0/100
Data completeness
3/8 — Basic
Drug data last refreshed 5h ago · AI intelligence enriched 8h ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
SUFLAVE is an oral polyelectrolyte solution containing polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride. It is a bowel cleansing agent indicated for colonoscopy preparation by inducing osmotic diarrhea to evacuate the colon. This is a non-absorbed electrolyte formulation designed to cleanse the bowel without systemic electrolyte imbalance.
$0.462MPart D
Peak18.1 years to LOEProduct is at peak lifecycle stage post-approval with emerging Medicare utilization; commercial team likely remains small given modest Part D claims volume.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Career Relevance
SUFLAVE currently has zero linked job openings, indicating a stable, lean commercial team post-launch. Career opportunities on this product are limited to specialized roles in market access, brand management, or field presence in gastroenterology channels.
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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.