Class II · Moderate risk
cimzia (certolizumab pegol)
Lack of Assurance of Sterility
National Drug Code
Is NDC 50474-0710-81 recalled?
Cimzia · 3 CARTON in 1 BOX (50474-710-81) / 2 SYRINGE, GLASS in 1 CARTON / 1 mL in 1 SYRINGE, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 50474-0710-81 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
- certolizumab pegol
- Strength
- CERTOLIZUMAB PEGOL 200 mg/mL
- Form
- Injection, Solution · Subcutaneous
- Labeler
- UCB, Inc.
- Type
- Human Prescription Drug
- Product code
- 50474-0710
Recalls naming this package
Class II · Moderate risk
Cimzia 200 mg/mL PFS Kit #2 NDC 50474-0710-79 28 days supply.
Lack of Processing Controls.
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
- 50474-0570 Briviact 1
- 50474-0597 Keppra 1
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