Class II ยท Moderate risk
Neupogen (filgrastim)
Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.
National Drug Code
Is NDC 55513-0546-10 recalled?
Neupogen · 10 VIAL in 1 BOX (55513-546-10) / 1.6 mL in 1 VIAL (55513-546-01)
Yes — this exact package was recalled
1 FDA recall names the code 55513-0546-10 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
- Filgrastim
- Strength
- FILGRASTIM 480 ug/1.6mL
- Form
- Injection, Solution · Intravenous, Subcutaneous
- Labeler
- Amgen, Inc
- Type
- Human Prescription Drug
- Product code
- 55513-0546
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
- 55513-0710 Prolia 3
- 55513-0073 Sensipar 2
- 55513-0074 Sensipar 2
- 55513-0075 Sensipar 1
- 55513-0206 Mvasi 1
- 55513-0530 Neupogen 1
Free recall alerts
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