SUFLAVE
polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution · KIT · Azurity Pharmaceuticals, Inc.
SUFLAVE is a kit containing polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution. Manufactured by Azurity Pharmaceuticals, Inc..
Key Facts
- Brand Name
- SUFLAVE
- Generic Name
- polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution
- NDC Code (Product)
24338-550- Manufacturer
- Azurity Pharmaceuticals, Inc.
- Dosage Form
- KIT
- Marketing Status
- Application #
- NDA215344
- Marketing Start
- 04/01/2026
Recall History
No Recall HistoryFrequently Asked Questions
What is SUFLAVE used for?
SUFLAVE contains polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution. It is a kit taken as directed. Consult your doctor for specific uses.
Is SUFLAVE a controlled substance?
SUFLAVE is not classified as a controlled substance by the DEA.
What is the generic name for SUFLAVE?
The generic name for SUFLAVE is polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution. There are no other listed brand versions of polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution.
What is the NDC code for SUFLAVE ?
The NDC (National Drug Code) for SUFLAVE is 24338-550, listed by Azurity Pharmaceuticals, Inc..
Other SUFLAVE Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)