Class III ยท Low risk
Selegiline HCL Tablets USP 5mg
Stason Pharmaceuticals is recalling Selegiline HCl tablets, USP 5mg 60 count bottle due to an out of specification result for dissolution of stability samples.
National Drug Code
Is NDC 51862-0146-06 recalled?
Selegiline HCL Tablets USP 5mg
Yes — this exact package was recalled
1 FDA recall names the code 51862-0146-06 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.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
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
- 51862-0159 See recall 1
- 51862-0185 See recall 1
- 51862-0186 See recall 1
- 51862-0295 Fabior 1
- 51862-0455 Clonidine 1
- 51862-0604 See recall 1
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