NDC 62756-202
gabapentin 600 mg tablet, film coated
On the label: Sun Pharmaceutical Industries, Inc..
FDA lists this product, but its label isn't on DailyMed yet, so we can't show its factories. They usually appear within a few weeks.
Where it's made
Recalls
- Mar 4, 2025 · Class III · Sun Pharmaceutical Industries Inc
Cross Contamination
Lots: Lot # a) HAD1458A, Exp. date 04/2025, HAD2718A, Exp. date 07/2025, b) HAD3432A, exp. date 08/2025 - Mar 4, 2025 · Class III · Sun Pharmaceutical Industries Inc
Cross Contamination
Lots: Lot # a) HAD1712B, Exp. date 03/2025 b) HAD1712C, exp. date 03/2025
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 ANDA077525
- On the market since
- Sep 1, 2022
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