NDC 70518-4532
Gabapentin 600 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Granules Pharmaceuticals Inc.'s NDC 70010-227.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Granules India Limited | Medchal-Malkajgiri District, India | Makes it, tests it and labels it | Problems found, fixed voluntarilyFeb 14, 2020 · 6 inspections |
Recalls
- Jul 31, 2024 · Class II · Granules Pharmaceuticals Inc.
Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were found in bottle of Gabapentin Tablets
Lots: Lot 1380040A, Exp. date July 31, 2025
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, film coated, oral
- Strength
- 600 mg
- Approval
- ANDA ANDA217116
- On the market since
- Dec 7, 2025
- Package NDCs
70518-4532-070518-4532-1- Official label
- DailyMed (National Library of Medicine), updated Oct 29, 2026
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