Class II · Moderate risk
Viatrexx-Ouch
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
National Drug Code
Is NDC 73069-0402-41 recalled?
Viatrexx-Ouch
Yes — this exact package was recalled
1 FDA recall names the code 73069-0402-41 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
- 73069-0024 See recall 1
- 73069-0035 See recall 1
- 73069-0037 See recall 1
- 73069-0039 See recall 1
- 73069-0095 See recall 1
- 73069-0100 See recall 1
Free recall alerts
Know the day your medication is recalled
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