Class III ยท Low risk
ERBITUX CETUXIMAB Injection
Labeling: Missing label; potential for missing primary container label on the vial.
National Drug Code
Is NDC 66733-0958-23 recalled?
Erbitux · 1 VIAL, SINGLE-DOSE in 1 CARTON (66733-958-23) / 100 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 66733-0958-23 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
- cetuximab
- Strength
- CETUXIMAB 2 mg/mL
- Form
- Solution · Intravenous
- Labeler
- ImClone LLC
- Type
- Human Prescription Drug
- Product code
- 66733-0958
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.
Free recall alerts
Know the day your medication is recalled
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