# Polyethylene Glycol

NDC: 68001-505
Generic name: Polyethylene Glycol
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20210618

FDA application: ANDA091077

## 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:"68001-505"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-505
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c4cae70c-68da-0bbc-e053-2a95a90a395a