NDC 52268-101
GoLYTELY 5 ingredients powder, for solution
On the label: Braintree Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Braintree Laboratories, Inc. | Holbrook, MA, United States | Makes it | No problems foundMar 7, 2025 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Polyethylene Glycol 3350 and Potassium Cation and Sodium Cation: every company that makes it
- Form
- powder, for solution
- Strength
- 5 ingredients
- Approval
- NDA NDA019011
- On the market since
- Jul 13, 1984
- Package NDCs
52268-101-01- Official label
- DailyMed (National Library of Medicine), updated Oct 8, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?