Class II · Moderate risk
National Drug Code
Is NDC 71384-0340-08 recalled?
Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic Solution 1%
Yes — this exact package was recalled
1 FDA recall names the code 71384-0340-08 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.
1 of these recalls is still ongoing.
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
- 71384-0640 See recall 4
- 71384-0512 See recall 2
- 71384-0513 See recall 2
- 71384-0514 See recall 2
- 71384-0733 See recall 2
- 71384-0310 See recall 1
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