# TRILYTE

NDC: 84386-013
Generic name: polyethylene glyocol 3350, sodium chloride, sodium bicarbonate and potassium chloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20260414

FDA application: ANDA076491

## Active ingredients

- POLYETHYLENE GLYCOL 3350: 420 g/4L
- POTASSIUM CHLORIDE: 1.48 g/4L
- SODIUM BICARBONATE: 5.72 g/4L
- SODIUM CHLORIDE: 11.2 g/4L

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84386-013"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84386-013
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=79f5e596-8d51-4227-afcc-f5e341150957