NDC 10122-100

FERRIPROX

Deferiprone

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.

• Product ID: 10122-100_7c82e2f1-fe2d-4412-8d12-e5da5cedb9e9
• NDC: 10122-100
• Product Type: Human Prescription Drug
• Proprietary Name: FERRIPROX
• Generic Name: Deferiprone
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2011-11-25
• Marketing Category: NDA / NDA
• Application Number: NDA021825
• Labeler Name: Chiesi USA, Inc.
• Substance Name: DEFERIPRONE
• Active Ingredient Strength: 500 mg/1
• Pharm Classes: Iron Chelating Activity [MoA],Iron Chelator [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 10122-100-10

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10122-100-10)

• Marketing Start Date: 2021-01-01
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "FERRIPROX" or generic name "Deferiprone"

NDC	Brand Name	Generic Name
10122-100	FERRIPROX	deferiprone
10122-101	FERRIPROX	deferiprone
10122-103	FERRIPROX	DEFERIPRONE
10122-104	FERRIPROX	deferiprone
52609-0006	FERRIPROX	deferiprone
52609-0007	FERRIPROX	deferiprone
52609-4502	FERRIPROX	deferiprone
0054-0576	Deferiprone	Deferiprone
0054-0711	Deferiprone	Deferiprone
51672-4196	Deferiprone	Deferiprone