NDC 24338-236
GoLYTELY 5 ingredients powder, for solution
On the label: Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals).
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) names for other drugs.
Product details
- Generic drug
- Polyethylene Glycol 3350 and Potassium Cation and Sodium Cation: every company that makes it
- Form
- powder, for solution, oral
- Strength
- 5 ingredients
- Approval
- NDA NDA019011
- On the market since
- Apr 17, 2026
- Package NDCs
24338-236-01- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2026
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