Class II · Moderate risk
Amoxicillin for Oral Suspension
Microbial Contamination of Non-Sterile Products: Suspensions made from these lots of Amoxicillin 125 mg/5 mL showed yeast and mold growth at the 14 day time point.
National Drug Code
Is NDC 43598-0222-80 recalled?
Amoxicillin for Oral Suspension
Yes — this exact package was recalled
1 FDA recall names the code 43598-0222-80 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
- 43598-0315 Amlodipine besylate and Atorvastatin calcium 2
- 43598-0405 Phytonadione Phytonadione 2
- 43598-0477 See recall 2
- 43598-0510 Esomeprazole Magnesium 2
- 43598-0561 Lansoprazole 2
- 43598-0743 Ezetimibe and Simvastatin 2
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