Class II ยท Moderate risk
Allopurinol Tablets 100mg
Presence of Foreign Substance: manufacturer recalled this re-packaged product due to reports of a small piece of green plastic embedded in the crack towards the edge of the tablet.
National Drug Code
Is NDC 68788-7383-09 recalled?
Allopurinol Tablets 100mg
Yes — this exact package was recalled
1 FDA recall names the code 68788-7383-09 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
- 68788-6932 See recall 3
- 68788-0048 See recall 2
- 68788-7758 See recall 2
- 68788-0841 See recall 1
- 68788-6381 See recall 1
- 68788-6382 See recall 1
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