Class II · Moderate risk
Voriconazole Tablets
cGMP Deviations: Received notification from their supplier requesting they perform a recall due to the fact they repackaged the product.
National Drug Code
Is NDC 60687-0294-11 recalled?
Voriconazole Tablets
Yes — this exact package was recalled
1 FDA recall names the code 60687-0294-11 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
- 60687-0423 Clobazam 2
- 60687-0695 See recall 2
- 60687-0106 See recall 1
- 60687-0112 Anastrozole 1
- 60687-0133 See recall 1
- 60687-0139 See recall 1
Free recall alerts
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