NDC 71205-514
Gabapentin 800 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP 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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA205101
- On the market since
- Feb 4, 2016
- Package NDCs
71205-514-3071205-514-6071205-514-90- Official label
- DailyMed (National Library of Medicine), updated Apr 1, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?