# Polyethylene Glycol 3350

NDC: 50844-772
Generic name: Polyethylene Glycol 3350
Labeler / Manufacturer: L.N.K. International, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20260910

FDA application: ANDA217505

## Active ingredients

- POLYETHYLENE GLYCOL 3350: 17 g/17g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50844-772"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50844-772
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bbc11078-73f7-4d27-b0d3-4d4ae5dae240