Class II · Moderate risk
BroveX PSB LIQUID
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
National Drug Code
Is NDC 58605-0150-02 recalled?
BroveX PSB LIQUID
Yes — this exact package was recalled
1 FDA recall names the code 58605-0150-02 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
- 58605-0151 See recall 1
- 58605-0408 See recall 1
- 58605-0409 See recall 1
- 58605-0440 See recall 1
- 58605-0441 See recall 1
Free recall alerts
Know the day your medication is recalled
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