Class III · Low risk
Clonazepam Tablets
Failed Impurities/Degradation Specifications: out of specification result for Clonazepam Related Compound (RC) A (a known impurity) at 15 month timepoint.
National Drug Code
Is NDC 51079-0881-20 recalled?
Clonazepam Tablets
Yes — this exact package was recalled
1 FDA recall names the code 51079-0881-20 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
Class III · Low risk
Clonazepam Tablets
Failed Impurities/Degradation Specifications: out of specification result for known impurity at 6 month timepoint.
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
- 51079-0443 Levothyroxine Sodium 2
- 51079-0445 Levothyroxine Sodium 2
- 51079-0947 See recall 2
- 51079-0020 See recall 1
- 51079-0088 Mirtazapine 1
- 51079-0090 See recall 1
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