NDC 67046-1536
Gabapentin 800 mg tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-178.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA205101
- On the market since
- Mar 25, 2025
- Package NDCs
67046-1536-3- Official label
- DailyMed (National Library of Medicine), updated Mar 25, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?