# GAVILYTE-N

NDC: 43386-050
Generic name: polyethylene glycol-3350, sodium chloride, potassium chloride and sodium bicarbonate
Labeler / Manufacturer: Lupin Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20090528

FDA application: ANDA090019

## Active ingredients

- POLYETHYLENE GLYCOL 3350: 420 g/438.4g
- POTASSIUM CHLORIDE: 1.48 g/438.4g
- SODIUM BICARBONATE: 5.72 g/438.4g
- SODIUM CHLORIDE: 11.2 g/438.4g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43386-050"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43386-050
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=27195187-75a3-431f-90d9-84da1b94e849