Class II · Moderate risk
fentaNYL 5000 mcg/250 mL
Lack of Assurance of Sterility: Firm received fentanyl from a supplier who recalled it because fliptop vial crimps were loose or missing.
National Drug Code
Is NDC 75901-8015-04 recalled?
fentaNYL 5000 mcg/250 mL
Yes — this exact package was recalled
1 FDA recall names the code 75901-8015-04 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
- 75901-8008 See recall 2
- 75901-1205 See recall 1
- 75901-7210 See recall 1
- 75901-8002 See recall 1
- 75901-8007 See recall 1
Free recall alerts
Know the day your medication is recalled
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