Class II ยท Moderate risk
Nelarabine Injection
Failed Impurities/Degradation Specifications
National Drug Code
Is NDC 70710-1726-01 recalled?
Nelarabine · 1 VIAL, SINGLE-DOSE in 1 CARTON (70710-1726-1) / 50 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 70710-1726-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Nelarabine
- Strength
- NELARABINE 5 mg/mL
- Form
- Injection · Intravenous
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 70710-1726
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
- 70710-1592 icosapent ethyl 3
- 70710-1129 Chlorpromazine hydrochloride 2
- 70710-1047 Erythromycin 1
- 70710-1048 Erythromycin 1
- 70710-1130 Chlorpromazine hydrochloride 1
- 70710-1131 Chlorpromazine hydrochloride 1
Free recall alerts
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