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FDA Drug information

Nelarabine

Read time: 1 mins
Marketing start date: 28 Apr 2024

Summary of product characteristics


Effective Time

20221105

Version

2

Spl Product Data Elements

Nelarabine Nelarabine NELARABINE NELARABINE HYDROCHLORIC ACID SODIUM CHLORIDE SODIUM HYDROXIDE WATER

Application Number

ANDA215037

Brand Name

Nelarabine

Generic Name

Nelarabine

Product Ndc

70771-1685

Product Type

HUMAN PRESCRIPTION DRUG

Route

INTRAVENOUS

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1685-1 Nelarabine Injection 250 mg/5 mL (5 mg/mL) 50 mL Single-Dose Vial For Intravenous Infusion Only Rx Only NDC 70771-1685-1 Nelarabine Injection 250 mg/5 mL (5 mg/mL) 50 mL Single-Dose Vial Carton For Intravenous Infusion Only Rx Only vial label

Spl Unclassified Section

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