NDC 71610-463
Gabapentin 600 mg tablet
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-177.
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
- Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN, United States · repackages it
Recalls
- Feb 17, 2023 · Class III · Sciegen Pharmaceuticals Inc
Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.
Lots: Lot # G177092, Exp. 11/24
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- tablet
- Strength
- 600 mg
- Approval
- ANDA ANDA205101
- On the market since
- Feb 4, 2016
- Package NDCs
71610-463-3071610-463-4571610-463-5371610-463-6071610-463-7071610-463-7371610-463-8071610-463-92- Official label
- DailyMed (National Library of Medicine), updated Nov 12, 2020
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