# GOLYTELY
> **NDA019011** · New Drug Application · Sponsor: AZURITY · Approved 1984-07-13
## Drug
- **FDA Application Number:** NDA019011
- **Application type:** New Drug Application
- **Brand name:** GOLYTELY
- **Generic name:** POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE
- **Active ingredients:** POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
- **Dosage form:** FOR SOLUTION
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** AZURITY
- **Manufacturer:** Braintree Laboratories, Inc.
- **First approval:** 1984-07-13
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=019011)
---
*MORVS · CC0 1.0*