Class II · Moderate risk
Zonisamide Capsules
CGMP Deviations: Firm did not adequately investigate customer complaints.
National Drug Code
Is NDC 64679-0990-01 recalled?
Zonisamide Capsules
Yes — this exact package was recalled
2 FDA recalls name the code 64679-0990-01 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 II · Moderate risk
ZONISAMIDE Capsule
Labeling: Label Mixup; ZONISAMIDE Capsule, 100 mg may be potentially mislabeled as PHYTONADIONE, Tablet, 5 mg, NDC 25010040515, Pedigree: W003737, EXP: 5/31/2014.
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
- 64679-0735 See recall 3
- 64679-0904 See recall 3
- 64679-0434 See recall 2
- 64679-0714 See recall 2
- 64679-0736 See recall 2
- 64679-0737 See recall 2
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