Class II · Moderate risk
0.45% Sodium Chloride Injection USP
Labeling: Wrong Bar Code; Bar code scans as 0.15% Potassium Chloride in 0.9% Sodium Chloride (20 mEq K/liter).
National Drug Code
Is NDC 0264-7802-00 recalled?
Sodium Chloride · 12 CONTAINER in 1 CASE (0264-7802-00) / 1000 mL in 1 CONTAINER
Yes — this exact package was recalled
1 FDA recall names the code 0264-7802-00 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.
- Active ingredient
- Sodium Chloride
- Strength
- SODIUM CHLORIDE .45 g/100mL
- Form
- Injection, Solution · Intravenous
- Labeler
- B. Braun Medical Inc.
- Type
- Human Prescription Drug
- Product code
- 0264-7802
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
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