# GoLYTELY

NDC: 24338-236
Generic name: Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20260417

FDA application: NDA019011

## Active ingredients

- POLYETHYLENE 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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24338-236"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24338-236
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7609ecf7-0ce0-4fbb-9c27-30987f689575