Class II · Moderate risk
0.9% Sodium Chloride Injection
Lack of Assurance of Sterility
National Drug Code
Is NDC 65219-0468-05 recalled?
Sodium chloride
Yes — this exact package was recalled
1 FDA recall names the code 65219-0468-05 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.
1 of these recalls is still ongoing.
- Active ingredient
- Sodium Chloride
- Strength
- SODIUM CHLORIDE 9 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Fresenius Kabi USA, LLC
- Type
- Human Prescription Drug
- Product code
- 65219-0468
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
- 65219-0282 Sodium chloride 1
- 65219-0432 Sodium Chloride 1
- 65219-0456 Dextrose 1
- 65219-0458 Dextrose 1
- 65219-0464 Dextrose 1
- 65219-0466 Sodium chloride 1
Free recall alerts
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