Class III · Low risk
DULOXETINE Delayed-Release Capsules
Labeling; Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on container label is 02/2019, correct expiration date should be 02/2018
National Drug Code
Is NDC 60429-0166-10 recalled?
DULOXETINE Delayed-Release Capsules
Yes — this exact package was recalled
1 FDA recall names the code 60429-0166-10 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
- 60429-0316 See recall 4
- 60429-0317 See recall 4
- 60429-0318 See recall 3
- 60429-0640 See recall 2
- 60429-0641 See recall 2
- 60429-0642 See recall 2
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