NDC 52609-0007

FERRIPROX

Deferiprone

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

• Product ID: 52609-0007_1d15b719-6cf5-1742-2ff4-0db8aa699c93
• NDC: 52609-0007
• Product Type: Human Prescription Drug
• Proprietary Name: FERRIPROX
• Generic Name: Deferiprone
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2019-08-01
• Marketing Category: NDA / NDA
• Application Number: NDA021825
• Labeler Name: ApoPharma 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: 2020-12-31

Packaging

NDC 52609-0007-5

50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52609-0007-5)

• Marketing Start Date: 2019-08-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 52609-0007-5 [52609000705]

FERRIPROX TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA021825
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2019-08-01

Drug Details

Active Ingredients

Ingredient	Strength
DEFERIPRONE	1000 mg/1

OpenFDA Data

• SPL SET ID: 57bd50e6-c948-0037-4a4b-c8951f70d04a
• Manufacturer:
  • ApoPharma USA, Inc.
• UNII:
  • 2BTY8KH53L
• RxNorm Concept Unique ID - RxCUI:
  • 2180999
  • 2180997

Pharmacological Class

• Iron Chelating Activity [MoA]
• Iron Chelator [EPC]

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