Class III ยท Low risk
Gabapentin Tablets USP
Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.
National Drug Code
Is NDC 76282-0405-05 recalled?
Gabapentin · 500 TABLET, FILM COATED in 1 BOTTLE (76282-405-05)
Yes — this exact package was recalled
1 FDA recall names the code 76282-0405-05 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- gabapentin
- Strength
- GABAPENTIN 600 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Exelan Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 76282-0405
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 76282-0478 Lanthanum carbonate 2
- 76282-0103 Diclofenac Sodium 1
- 76282-0673 Ramipril 1
- 76282-0708 See recall 1
Free recall alerts
Know the day your medication is recalled
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