Class III ยท Low risk
LEUKINE (Sargramostim)
FAILED STABILITY SPECIFICATION: Out-of-specification (OOS) result observed for Leukine (sargramostim) at the 27-month stability timepoint.
National Drug Code
Is NDC 71837-5843-05 recalled?
Leukine · 5 VIAL, SINGLE-DOSE in 1 CARTON (71837-5843-5) / 1 mL in 1 VIAL, SINGLE-DOSE (71837-5843-1)
Yes — this exact package was recalled
1 FDA recall names the code 71837-5843-05 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
- Sargramostim
- Strength
- SARGRAMOSTIM 250 ug/mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous, Subcutaneous
- Labeler
- Partner Therapeutics, Inc.
- Type
- Human Prescription Drug
- Product code
- 71837-5843
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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