NDC 43386-090
Gavilyte Gtm 5 ingredients powder, for solution
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Novel Laboratories, Inc. | Somerset, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride and Sodium Bicarbo: every company that makes it
- Form
- powder, for solution, oral
- Strength
- 5 ingredients
- Approval
- ANDA ANDA090231
- On the market since
- Jun 1, 2009
- Package NDCs
43386-090-19- Official label
- DailyMed (National Library of Medicine), updated Sep 10, 2025
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