Class II · Moderate risk
Benicar Tablets
Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping
National Drug Code
Is NDC 65597-0103-30 recalled?
Benicar Tablets
Yes — this exact package was recalled
1 FDA recall names the code 65597-0103-30 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
- 65597-0701 See recall 2
- 65597-0104 See recall 1
- 65597-0105 See recall 1
- 65597-0106 See recall 1
- 65597-0107 See recall 1
- 65597-0113 See recall 1
Free recall alerts
Know the day your medication is recalled
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