Class II ยท Moderate risk
VELCADE (bortezomib)
Defective Container: Confirmed reports of loose vial crimps.
National Drug Code
Is NDC 63020-0049-01 recalled?
Velcade · 1 VIAL in 1 CARTON (63020-049-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 63020-0049-01 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
- bortezomib
- Strength
- BORTEZOMIB 3.5 mg/1
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous, Subcutaneous
- Labeler
- Takeda Pharmaceuticals America, Inc.
- Type
- Human Prescription Drug
- Product code
- 63020-0049
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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