NDC 85509-2180
Gabapentin 300 mg capsule
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-180.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals India Private Limited | Mahabubnagar, India | Makes it and tests it | Not inspected on record |
| 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
- Phoenix RX LLC, Hatboro, PA, United States · repackages it and relabels it
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- capsule, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA204989
- On the market since
- Feb 18, 2016
- Package NDCs
85509-2180-185509-2180-385509-2180-685509-2180-9- Official label
- DailyMed (National Library of Medicine), updated Apr 16, 2026
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