Class III · Low risk
Metoprolol Tartrate Injection
Failed pH Specifications: High Out-of-Specification results for pH were obtained during stability testing.
National Drug Code
Is NDC 70518-0868-00 recalled?
Metoprolol Tartrate Injection
Yes — this exact package was recalled
1 FDA recall names the code 70518-0868-00 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
- 70518-1220 See recall 2
- 70518-1560 Doxazosin 2
- 70518-3519 See recall 2
- 70518-3772 Clindamycin Hydrochloride 2
- 70518-0060 See recall 1
- 70518-0064 See recall 1
Free recall alerts
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