Ferriprox 500 mg Three-Times-A-Day Oral Tablet
RxNorm 1190357 NDC Crossover

NDC Directory Crossover & Product Mapping

The following National Drug Codes (NDCs) are directly associated with the clinical concept for Ferriprox 500 mg Three-Times-A-Day Oral Tablet (RxCUI 1190357). This crossover tool provides a verified mapping between standardized RxNorm clinical drug definitions and the specific manufactured products listed in the FDA NDC directory.

Healthcare professionals, pharmacists, and data analysts use this list to identify various brand names, labelers, and commercial packaging variations linked to this semantic clinical drug concept. Each entry below represents a commercial product that fulfills the requirements of this specific clinical identifier.

Manufacturer Quick Index

→ ApoPharma USA, Inc. 1
→ Chiesi USA, Inc. 3

ApoPharma USA, Inc.

NDC Product

Ferriprox
NDC 52609-0006

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Excluded / Inactive

Chiesi USA, Inc.

NDC Product

Ferriprox
NDC 10122-100

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Ferriprox
NDC 10122-103

Generic Name
Deferiprone
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Ferriprox
NDC 10122-104

Generic Name
Deferiprone
Dosage Form
Tablet
Route
Oral
Marketing
NDA
Active Listing