# GaviLyte-H and Bisacodyl

NDC: 43386-071
Generic name: Polyethylene Glycol 3350, Sodium Chloride, Sodium Bicarbonate, Potassium Chloride and Bisacodyl Delayed-release Tablet
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: ORAL
Marketing started: 20150421

FDA application: ANDA202217

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43386-071"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43386-071
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=78fe1c29-e22a-4615-a2f9-a61cd4eb38a3