Class II ยท Moderate risk
Arthrotec 75
Tablet Separation: The manufacturer of Arthrotec had recalled the lots that were used to re-package this product because they may contain broken tablets.
National Drug Code
Is NDC 54868-4165-01 recalled?
Arthrotec 75
Yes — this exact package was recalled
1 FDA recall names the code 54868-4165-01 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
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
- 54868-0024 See recall 1
- 54868-0025 See recall 1
- 54868-0031 See recall 1
- 54868-0158 See recall 1
- 54868-0816 See recall 1
- 54868-2913 See recall 1
Free recall alerts
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