Class II ยท Moderate risk
Dupixent 300 mg/2 mL PFS #2 w/ NS NDC 00024-5914-01 28 days supply
Lack of Processing Controls.
National Drug Code
Is NDC 0024-5914-01 recalled?
Dupixent · 2 SYRINGE, GLASS in 1 CARTON (0024-5914-01) / 2 mL in 1 SYRINGE, GLASS (0024-5914-00)
Yes — this exact package was recalled
1 FDA recall names the code 0024-5914-01 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
- Dupilumab
- Strength
- DUPILUMAB 300 mg/2mL
- Form
- Injection, Solution · Subcutaneous
- Labeler
- Sanofi-Aventis U.S. LLC
- Type
- Human Prescription Drug
- Product code
- 0024-5914
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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