Class I ยท High risk
Citrulline
Labeling: Label Mix-Up: FDA tested samples of API from Medisca, labeled as to contain L-Citrulline, and results revealed no L-Citrulline was present. Levels of N-acetyl-leucine were found instead.
National Drug Code
Is NDC 38779-1186-04 recalled?
Citrulline
Yes — this exact package was recalled
1 FDA recall names the code 38779-1186-04 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
- 38779-0732 Estriol 1
- 38779-0869 Estradiol 1
- 38779-0891 See recall 1
- 38779-0989 See recall 1
- 38779-2261 See recall 1
- 38779-2673 See recall 1
Free recall alerts
Know the day your medication is recalled
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