NDC 21695-059
Gabapentin 800 mg tablet, film coated
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Sun Pharmaceutical Industries, Inc.'s NDC 62756-204.
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.
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
- Strength
- 800 mg
- Approval
- ANDA ANDA077525
- On the market since
- Aug 24, 2006
- Package NDCs
21695-059-3021695-059-6021695-059-90- Official label
- DailyMed (National Library of Medicine), updated Oct 23, 2009
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?