GoLYTELY 236 g/4L
Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride · POWDER, FOR SOLUTION · Azurity Pharmaceuticals, Inc.
GoLYTELY is a powder, for solution containing polyethylene glycol 3350, sodium sulfate anhydrous, sodium bicarbonate, sodium chloride, potassium chloride at 236 g/4L, taken oral. Manufactured by Azurity Pharmaceuticals, Inc..
Key Facts
- Brand Name
- GoLYTELY
- Generic Name
- Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride
- NDC Code (Product)
24338-236- Manufacturer
- Azurity Pharmaceuticals, Inc.
- Strength
- 236 g/4L
- Dosage Form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Marketing Status
- Application #
- NDA019011
- Drug Class
- Osmotic Laxative [EPC]
- Marketing Start
- 04/17/2026
Recall History
No Recall HistoryFrequently Asked Questions
What is GoLYTELY used for?
GoLYTELY contains Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride. It is a powder, for solution taken oral. Consult your doctor for specific uses.
Is GoLYTELY a controlled substance?
GoLYTELY is not classified as a controlled substance by the DEA.
What is the generic name for GoLYTELY?
The generic name for GoLYTELY is Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride. There are 3 other brand versions of Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride.
What is the NDC code for GoLYTELY 236 g/4L?
The NDC (National Drug Code) for GoLYTELY 236 g/4L is 24338-236, listed by Azurity Pharmaceuticals, Inc..