Class II ยท Moderate risk
Granix (tbo-filgrastim)
Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit
National Drug Code
Is NDC 63459-0910-15 recalled?
Granix · 10 BLISTER PACK in 1 CARTON (63459-910-15) / 1 SYRINGE, GLASS in 1 BLISTER PACK (63459-910-12) / .5 mL in 1 SYRINGE, GLASS (63459-910-01)
Yes — this exact package was recalled
1 FDA recall names the code 63459-0910-15 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
- tbo-filgrastim
- Strength
- FILGRASTIM 300 ug/.5mL
- Form
- Injection, Solution · Subcutaneous
- Labeler
- Cephalon, LLC
- Type
- Human Prescription Drug
- Product code
- 63459-0910
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
- 63459-0348 Bendeka 1
- 63459-0502 See recall 1
Free recall alerts
Know the day your medication is recalled
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