Class I ยท High risk
Morphine Sulfate PF 25 mg/25mL
Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A
National Drug Code
Is NDC 73177-0105-04 recalled?
Morphine Sulfate PF 25 mg/25mL
Yes — this exact package was recalled
1 FDA recall names the code 73177-0105-04 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
- 73177-0104 See recall 2
- 73177-0102 See recall 1
- 73177-0109 See recall 1
- 73177-0156 See recall 1
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