Class II ยท Moderate risk
BENLYSTA (belimumab)
CGMP Deviations; potential temperature excursions due to transit delays
National Drug Code
Is NDC 49401-0102-01 recalled?
Benlysta · 1 VIAL in 1 CARTON (49401-102-01) / 5 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 49401-0102-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- belimumab
- Strength
- BELIMUMAB 400 mg/5mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- GlaxoSmithKline LLC
- Type
- Human Prescription Drug
- Product code
- 49401-0102
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
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