Labetalol Hydrochloride Injection
Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.
National Drug Code
Labetalol Hydrochloride Injection
1 FDA recall names the code 0409-2267-25 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.
Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.
Presence of Particulate Matter; metal embedded in the glass vial and visible particles floating in the solution
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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