Class II · Moderate risk
Cefazolin for injection USP
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 0264-3103-11 recalled?
Cefazolin Sodium · 24 CONTAINER in 1 CASE (0264-3103-11) / 50 mL in 1 CONTAINER
Yes — this exact package was recalled
2 FDA recalls name the code 0264-3103-11 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
- Cefazolin Sodium
- Strength
- CEFAZOLIN SODIUM 1 g/50mL
- Form
- Solution · Intravenous
- Labeler
- B. Braun Medical Inc.
- Type
- Human Prescription Drug
- Product code
- 0264-3103
Recalls naming this package
Class I · High risk
Cefazolin for Injection USP and Dextrose Injections USP
Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
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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