NDC 24338-236 – GoLYTELY

Polyethylene Glycol 3350 236 g/4L; Sodium Sulfate Anhydrous 22.74 g/4L; Sodium Bicarbonate 6.74 g/4L; Sodium Chloride 5.86 g/4L; Potassium Chloride 2.97 g/4L · Powder, For Solution · Oral

Human Prescription Drug

Product NDC24338-236

Product details

Brand name
GoLYTELY
Generic name
Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
Powder, For Solution
Route
Oral
Marketing category
NDA · NDA019011
Marketed since
April 17, 2026
Listing expires
December 31, 2027
Pharmacologic class
Osmotic Laxative; Osmotic Laxative; Osmotic Laxative; Osmotic Laxative; Osmotic Laxative; Potassium Salt

Active ingredients

Uses, dosage, side effects and warnings for GoLYTELY →

Package NDC codes (1)

Package NDCDescriptionSince
24338-236-014 L in 1 BOTTLE, PLASTIC (24338-236-01)Apr 17, 2026

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