NDC 51672-4196

Deferiprone

Deferiprone

Deferiprone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Taro Pharmaceuticals U.s.a., Inc.. The primary component is Deferiprone.

• Product ID: 51672-4196_4028eb31-5ba4-4626-9f1c-32e913896561
• NDC: 51672-4196
• Product Type: Human Prescription Drug
• Proprietary Name: Deferiprone
• Generic Name: Deferiprone
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2019-02-08
• Marketing Category: ANDA / ANDA
• Application Number: ANDA208800
• Labeler Name: Taro Pharmaceuticals U.S.A., 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: 2021-12-31

Packaging

NDC 51672-4196-1

100 TABLET in 1 BOTTLE (51672-4196-1)

• Marketing Start Date: 2019-02-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51672-4196-1 [51672419601]

Deferiprone TABLET

• Marketing Category: ANDA
• Application Number: ANDA208800
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-02-08

Drug Details

Active Ingredients

Ingredient	Strength
DEFERIPRONE	500 mg/1

OpenFDA Data

• SPL SET ID: 5af1643d-4c6e-4668-ae9b-1046f0ad6d8a
• Manufacturer:
  • Taro Pharmaceuticals U.S.A., Inc.
• UNII:
  • 2BTY8KH53L
• RxNorm Concept Unique ID - RxCUI:
  • 389242
• UPC Code:
  • 0351672419615

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
0054-0576	Deferiprone	Deferiprone
0054-0711	Deferiprone	Deferiprone
51672-4196	Deferiprone	Deferiprone
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