Class II · Moderate risk
Acetaminophen Tablets
CGMP Deviations: The recalled acetaminophen tablet lot was not manufactured under current good manufacturing practices as noted by a recent inspection of the manufacturing firm.
National Drug Code
Is NDC 10135-0152-01 recalled?
Acetaminophen Tablets
Yes — this exact package was recalled
1 FDA recall names the code 10135-0152-01 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
- 10135-0639 Levocetirizine Dihydrochloride 1
- 10135-0691 See recall 1
- 10135-0747 Digoxin 1
- 10135-0748 Digoxin 1
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