United States · FDA National Drug Code directory
FERRIPROX
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
- 10122-103_f6d7984f-011e-4a3f-bcf5-6a5b2b6ef2f9
- Product NDC
- 10122-103
- Form
- TABLET, FILM COATED
- Composition / generic term
- DEFERIPRONE
- Labeler
- Chiesi USA, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20190801
- Source listing expiry
- 20271231
Source-listed ingredients
- DEFERIPRONE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10122-103-05) · 10122-103-05
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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