Search by Drug Name or NDC

NDC 10122-0100-10 FERRIPROX 500 mg/1 Details

FERRIPROX 500 mg/1

FERRIPROX is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chiesi USA, Inc.. The primary component is DEFERIPRONE.

MedlinePlus Drug Summary

Deferiprone is used to remove excess iron in the body in adults and children 3 years of age and older who have thalassemia (an inherited condition that causes a low number of red blood cells). It is also used to remove excess iron in adults and children 3 years of age and older with sickle cell disease (an inherited blood disease) or other types of anemia (a lower than normal number of red blood cells). Deferiprone is in a class of medications called iron chelators. It works by attaching to iron in the body so that it can be excreted (removed from the body).

Related Packages: 10122-0100-10
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Deferiprone

Product Information

NDC	10122-0100
Product ID	10122-100_4f6573ca-2d61-4602-8a51-f9e30af2e489
Associated GPIs	93100028000320
GCN Sequence Number	046924
GCN Sequence Number Description	deferiprone TABLET 500 MG ORAL
HIC3	C8A
HIC3 Description	METALLIC POISON,AGENTS TO TREAT
GCN	84849
HICL Sequence Number	018544
HICL Sequence Number Description	DEFERIPRONE
Brand/Generic	Brand
Proprietary Name	FERRIPROX
Proprietary Name Suffix	n/a
Non-Proprietary Name	deferiprone
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	DEFERIPRONE
Labeler Name	Chiesi USA, Inc.
Pharmaceutical Class	Iron Chelating Activity [MoA], Iron Chelator [EPC]
DEA Schedule	n/a
Marketing Category	NDA
Application Number	NDA021825
Listing Certified Through	2024-12-31

Package

NDC 10122-0100-10 (10122010010)

Pricing Information	N/A
NDC Package Code	10122-100-10
Billing NDC	10122010010
Package	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10122-100-10)
Marketing Start Date	2021-01-01
NDC Exclude Flag	N