NDC 70710-1726 – Nelarabine

Nelarabine 5 mg/mL · Injection · Intravenous

Human Prescription Drug 1 recall

Product NDC70710-1726

Product details

Brand name
Nelarabine
Generic name
Nelarabine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA215037
Marketed since
November 17, 2021
Listing expires
December 31, 2026
Pharmacologic class
Nucleoside Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Nelarabine →

Package NDC codes (2)

Package NDCDescriptionSince
70710-1726-11 VIAL, SINGLE-DOSE in 1 CARTON (70710-1726-1) / 50 mL in 1 VIAL, SINGLE-DOSENov 17, 2021
70710-1726-86 VIAL, SINGLE-DOSE in 1 CARTON (70710-1726-8) / 50 mL in 1 VIAL, SINGLE-DOSENov 17, 2021

Recalls mentioning this NDC

Other Nelarabine products