Class II · Moderate risk
Walmart Amlodipine Besylate Tablets
Labeling: Label Error on Declared Strength-The recalled product has a misprint on the Amoldipine 10 mg label, 5 mg is listed in the USP description. Tablet strength is 10 mg.
National Drug Code
Is NDC 68645-0445-70 recalled?
Walmart Amlodipine Besylate Tablets
Yes — this exact package was recalled
1 FDA recall names the code 68645-0445-70 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
- 68645-0494 See recall 2
- 68645-0130 Fluoxetine 1
- 68645-0493 See recall 1
- 68645-0523 Sertraline Hydrochloride 1
- 68645-0545 See recall 1
- 68645-0577 See recall 1
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