# POLYETHYLENE GLYCOL 3350 NF

NDC: 11534-180
Generic name: polyethylene glycol 3350
Labeler / Manufacturer: SUNRISE PHARMACEUTICAL, INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20170613

FDA application: ANDA206105

## 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:"11534-180"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11534-180
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce5197a1-2677-4ffb-aef2-9221b28ebd23