United States · FDA National Drug Code directory

Desferal

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
0078-0467_9f58db85-c282-46eb-94ba-594e2092ddf2
Product NDC
0078-0467
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
deferoxamine mesylate
Labeler
Novartis Pharmaceuticals Corporation
Marketing category
NDA
Marketing start / end (source format)
19680402
Source listing expiry
20261231

Source-listed ingredients

  • DEFEROXAMINE MESYLATE — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 4 VIAL in 1 CARTON (0078-0467-91) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0078-0467-61) · 0078-0467-91

Source and coverage

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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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