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
70700-271_bb29f5e5-53df-4432-b6d1-854fa1e54d83
Product NDC
70700-271
Form
TABLET
Composition / generic term
Deferasirox
Labeler
Xiromed, LLC
Marketing category
ANDA
Marketing start / end (source format)
20200102
Source listing expiry
20261231

Source-listed ingredients

  • DEFERASIROX — 360 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE, PLASTIC (70700-271-30) · 70700-271-30

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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Deferasirox — United States | Molindra Medicines