0054-0711 : Deferiprone 1000 mg Oral Tablet, Coated


NDC0054-0711
Labeler: Hikma Pharmaceuticals USA Inc.
Product Type: Human Prescription Drug
Drug Name:  Deferiprone
Dosage Form: Oral Tablet, Coated
Application #: ANDA213239
Rev. Date: 


NDC Package Codes:

  • 0054-0711-19: 50 TABLET, COATED IN 1 BOTTLE (0054‑0711‑19)
  • 0054-0711-23: 150 TABLET, COATED IN 1 BOTTLE (0054‑0711‑23)
  • 0054-0711-28: 300 TABLET, COATED IN 1 BOTTLE (0054‑0711‑28)

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.
  • 0054-0576 Deferiprone 500 mg Oral Tablet, Coated by Hikma Pharmaceuticals USA Inc.
  • 51672-4196 Deferiprone 500 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.
  • 51672-4237 Deferiprone 1000 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 0054-0711 QR Code

< Prev: 0054-0710Next: 0054-0742 >




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.