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NDC 24338-236 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Generic namePolyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride
Labeler / ManufacturerAzurity Pharmaceuticals, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA019011
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsPOLYETHYLENE GLYCOL 3350 (236 g/4L)
POTASSIUM CHLORIDE (2.97 g/4L)
SODIUM BICARBONATE (6.74 g/4L)
SODIUM CHLORIDE (5.86 g/4L)
SODIUM SULFATE ANHYDROUS (22.74 g/4L)
Marketing started20260417
Package count1

External sources

Source: openFDA. Public-domain (CC0).