NDC 10122-103

FERRIPROX

Deferiprone

FERRIPROX is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Chiesi Usa, Inc.. The primary component is Deferiprone.

• Product ID: 10122-103_287670b2-60ba-4095-9fe3-7fab114bfc64
• NDC: 10122-103
• Product Type: Human Prescription Drug
• Proprietary Name: FERRIPROX
• Generic Name: Deferiprone
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2019-08-01
• Marketing Category: NDA /
• Application Number: NDA021825
• Labeler Name: Chiesi USA, Inc.
• Substance Name: DEFERIPRONE
• Active Ingredient Strength: 1000 mg/1
• Pharm Classes: Iron Chelating Activity [MoA],Iron Chelator [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 10122-103-05

50 TABLET in 1 BOTTLE, PLASTIC (10122-103-05)

• Marketing Start Date: 2019-08-01
• 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