United States · FDA National Drug Code directory

Cytarabine

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
61703-155_e3a8c0e9-19ed-49b7-8464-11e8806f47fd
Product NDC
61703-155
Form
INJECTION, SOLUTION
Composition / generic term
CYTARABINE
Labeler
Hospira, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20250407
Source listing expiry
20261231

Source-listed ingredients

  • CYTARABINE — 100 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-155-01) / 20 mL in 1 VIAL, SINGLE-DOSE · 61703-155-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →