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
59651-447_c220484e-1e6a-4a0c-a221-60223f3bc24c
Product NDC
59651-447
Form
GRANULE
Composition / generic term
DEFERASIROX
Labeler
Aurobindo Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20250908
Source listing expiry
20261231

Source-listed ingredients

  • DEFERASIROX — 90 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 PACKET in 1 CARTON (59651-447-30) / 1 GRANULE in 1 PACKET (59651-447-38) · 59651-447-30

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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