Class III ยท Low risk
Gabapentin Tablets
Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.
National Drug Code
Is NDC 50228-0177-05 recalled?
Gabapentin · 500 TABLET in 1 BOTTLE (50228-177-05)
Yes — this exact package was recalled
1 FDA recall names the code 50228-0177-05 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 · Oral
- Labeler
- ScieGen Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 50228-0177
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.
Free recall alerts
Know the day your medication is recalled
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