NDC 71610-069
gabapentin 600 mg tablet, film coated
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from Sun Pharmaceutical Industries, Inc.'s NDC 62756-202.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Sun Pharmaceutical Industries, Inc. names for other drugs.
Repackaging site
- Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN, United States · repackages it
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
- Aug 24, 2006
- Package NDCs
71610-069-4571610-069-6071610-069-8071610-069-92- Official label
- DailyMed (National Library of Medicine), updated Mar 21, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?