# NULYTELY
> **NDA019797** · New Drug Application · Sponsor: AZURITY · Approved 1991-04-22
## Drug
- **FDA Application Number:** NDA019797
- **Application type:** New Drug Application
- **Brand name:** NULYTELY
- **Generic name:** POLYETHYLENE GLYCOL 3350, SODIUM CHLORIDE, SODIUM BICARBONATE, POTASSIUM CHLORIDE
- **Active ingredients:** POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
- **Dosage form:** FOR SOLUTION
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** AZURITY
- **Manufacturer:** Wilshire Pharmaceuticals, Inc.
- **First approval:** 1991-04-22
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=019797)
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