NDC 72189-313
Gabapentin 600 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx 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
- Direct Rx, Dawsonville, GA, 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, oral
- Strength
- 600 mg
- Approval
- ANDA ANDA205101
- On the market since
- Jan 17, 2022
- Package NDCs
72189-313-6072189-313-7272189-313-90- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2025
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