Class II · Moderate risk Ongoing
Nelarabine Injection, 250mg/50mL, (5mg/mL), packaged in: a) 50 mL Single-Dose Vial, NDC 70710-1839-1; b) 6 x 50 mL Single-Dose…
Reason Failed Impurities/Degradation Specifications
Is Nelarabine recalled?
3 FDA recalls mention Nelarabine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Nelarabine.
Class II · Moderate risk Ongoing
Nelarabine Injection, 250mg/50mL, (5mg/mL), packaged in: a) 50 mL Single-Dose Vial, NDC 70710-1726-1; b) 6 x 50 mL Single-Dose…
Reason Failed Impurities/Degradation Specifications
Class II · Moderate risk Terminated
Arranon (nelarabine) Injection 5mg/mL, 50mL Vials, Rx only, For I.V. Infusion only, GlaxoSmith Kline, Research Triangle Park, NC…
Reason Impurities/Degradation Products: Potential for drug related impurities to exceed the specification limits.
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