Class II · Moderate risk
GSMS Incorporated
Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour timepoint.
National Drug Code
Is NDC 51407-0268-90 recalled?
Niacin · 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (51407-268-90)
Yes — this exact package was recalled
2 FDA recalls name the code 51407-0268-90 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.
2 of these recalls are still ongoing.
- Active ingredient
- Niacin
- Strength
- NIACIN 1000 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Golden State Medical Supply, Inc.
- Type
- Human Prescription Drug
- Product code
- 51407-0268
Recalls naming this package
Class II · Moderate risk
NIACIN Extended-Release Tablets
Failed Dissolution Specifications
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
- 51407-0097 See recall 1
- 51407-0098 See recall 1
- 51407-0129 See recall 1
- 51407-0192 Ezetimibe and Simvastatin 1
- 51407-0193 Ezetimibe and Simvastatin 1
- 51407-0215 Carbamazepine 1
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