National Drug Code
Metoprolol Succinate · 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-03)
2 FDA recalls name the code 68001-0501-03 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.
Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories.
Failed Dissolution Specifications
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.
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