United States · FDA National Drug Code directory

Deferasirox

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
45963-456_daefa0d6-0d5a-48fe-897b-cbc3e1db47f7
Product NDC
45963-456
Form
TABLET, FOR SUSPENSION
Composition / generic term
Deferasirox
Labeler
Actavis Pharma, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20190322 / 20260930

Source-listed ingredients

  • DEFERASIROX — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FOR SUSPENSION in 1 BOTTLE (45963-456-30) · 45963-456-30

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.

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