51672-4237 : Deferiprone 1000 mg Oral Tablet


NDC: 51672-4237
Labeler: Taro Pharmaceuticals U.S.a., Inc.
Product Type: Human Prescription Drug
Drug Name:  Deferiprone
Dosage Form: Oral Tablet
Application #: ANDA208800
Rev. Date: 


NDC Package Codes:

  • 51672-4237-4: 50 TABLET IN 1 BOTTLE (51672‑4237‑4)

Active Ingredients:

  • Deferiprone

Dosage Strength:

  • 1000 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 51672-4196 Deferiprone 500 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.
  • 0054-0576 Deferiprone 500 mg Oral Tablet, Coated by Hikma Pharmaceuticals USA Inc.
  • 0054-0711 Deferiprone 1000 mg Oral Tablet, Coated by Hikma Pharmaceuticals USA Inc.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.