Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 46163-0300-10 recalled?

Sodium Chloride · 12 BAG in 1 CARTON (46163-300-10) / 1000 mL in 1 BAG

Yes — this exact package was recalled

1 FDA recall names the code 46163-0300-10 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.

Active ingredient
Sodium Chloride
Strength
SODIUM CHLORIDE 900 mg/100mL
Form
Injection · Intravenous
Labeler
Fresenius Medical Care de Mexico, S.A. de C.V.
Type
Human Prescription Drug
Product code
46163-0300

Recalls naming this package

Class II · Moderate risk

Sodium Chloride 0.9%

Temperature Abuse: Product exposed to temperature outside specified limits.

Terminated Temperature excursion Fresenius Medical Care Holdings, Inc. NDC 46163-0300-10 D-0603-2021

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.