Drug Enforcement D-0256-2025

Failed Impurities/Degradation Specifications

Status

Ongoing

Classification

Class II

Report Date

March 12, 2025

Termination Date

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Product Information

Product description
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 Vial, NDC 70710-1839-8, Rx only, Manufactured by Zydus Lifesciences Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc, Pennington, NJ
Product quantity
1,893 vials
Reason for recall
Failed Impurities/Degradation Specifications
Recall initiation reason
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Initial firm notification
Letter
Distribution pattern
USA Nationwide

Location & Firm

Recalling firm
Zydus Pharmaceuticals (USA) Inc
Address
73 Route 31 N

United States
Voluntary / Mandated
Voluntary: Firm initiated
Status date
—

Codes & Dates

Recall number
D-0256-2025
Event ID
96291
Recall initiation date
February 13, 2025
Center classification date
March 6, 2025
Code info
Lot: a) P300197, Exp. Aug-2025; P400113, Exp. May-26; b) P300169, Exp. Jun-2025; P400115, Exp. May-2026.
More code info
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