United States · FDA National Drug Code directory

Deferoxamine mesylate

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
68083-173_d14a31c5-4e8d-4e3e-b38f-d73ffddfb629
Product NDC
68083-173
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Deferoxamine mesylate
Labeler
Gland Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20171009
Source listing expiry
20271231

Source-listed ingredients

  • DEFEROXAMINE MESYLATE — 2 g/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 4 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (68083-173-01) · 68083-173-01

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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