Class II ยท Moderate risk
AMGEN Kyprolis
Lack of Assurance of Sterility: Potential cracks in glass vials
National Drug Code
Is NDC 76075-0102-01 recalled?
Kyprolis · 1 VIAL, SINGLE-DOSE in 1 CARTON (76075-102-01) / 15 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 76075-0102-01 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.
- Active ingredient
- carfilzomib
- Strength
- CARFILZOMIB 30 mg/15mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Onyx Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 76075-0102
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.
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