NDC 70518-2912
Gabapentin 800 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-429.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it, tests it and packages it | No problems foundAug 30, 2019 · 6 inspections |
| Alkem Laboratories Limited | Baddi Solan, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
| VKT Pharma Private Limited | Srikakulam, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 7, 2025 · 2 inspections |
Product details
- Generic drug
- Gabapentin: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA206402
- On the market since
- Oct 20, 2020
- Package NDCs
70518-2912-070518-2912-170518-2912-270518-2912-3- Official label
- DailyMed (National Library of Medicine), updated Jul 30, 2026
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