Class II · Moderate risk
Acetaminophen suspension liquid
Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
National Drug Code
Is NDC 37205-0576-16 recalled?
Acetaminophen suspension liquid
Yes — this exact package was recalled
1 FDA recall names the code 37205-0576-16 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
- 37205-0185 See recall 1
- 37205-0372 See recall 1
- 37205-0550 See recall 1
- 37205-0577 See recall 1
- 37205-0745 See recall 1
- 37205-0987 See recall 1
Free recall alerts
Know the day your medication is recalled
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