Class II ยท Moderate risk
Opdualag (nivolumab and relatlimab-rmbw)
Lack of Assurance of Sterility.
National Drug Code
Is NDC 0003-7125-11 recalled?
Opdualag · 1 VIAL, SINGLE-DOSE in 1 CARTON (0003-7125-11) / 20 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 0003-7125-11 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.
1 of these recalls is still ongoing.
- Active ingredient
- nivolumab and relatlimab-rmbw
- Strength
- NIVOLUMAB 12 mg/mL; RELATLIMAB 4 mg/mL
- Form
- Injection · Intravenous
- Labeler
- E.R. Squibb & Sons, L.L.C.
- Type
- Human Prescription Drug
- Product code
- 0003-7125
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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