47781-624 : Deferoxamine Mesylate 2 g/1 Intramuscular; Intravenous; Subcutaneous Injection, Powder, Lyophilized, for Solution


NDC: 47781-624
Labeler: Alvogen Inc.
Product Type: Human Prescription Drug
Drug Name:  Deferoxamine Mesylate
Dosage Form: Intramuscular; Intravenous; Subcutaneous Injection, Powder, Lyophilized, for Solution
Application #: ANDA207384
Rev. Date: 


NDC Package Codes:

  • 47781-624-07: 1 VIAL IN 1 CARTON (47781‑624‑07) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION IN 1 VIAL

Active Ingredients:

  • Deferoxamine Mesylate

Dosage Strength:

  • 2 g/1

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
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  • 0409-2337 Deferoxamine Mesylate 2 g/1 Intramuscular; Intravenous; Subcutaneous Injection, Powder, Lyophilized, for Solution by Hospira, Inc.
  • 0555-1131 Deferoxamine Mesylate 2 g/20ml Intramuscular; Intravenous; Subcutaneous Injection, Powder, Lyophilized, for Solution by Barr Laboratories Inc.
  • 0555-1132 Deferoxamine Mesylate 500 mg/5ml Intramuscular; Intravenous; Subcutaneous Injection, Powder, Lyophilized, for Solution by Barr Laboratories Inc.
  • 52609-4504 Deferoxamine Mesylate 2 g/1 Intramuscular; Intravenous Injection, Powder, Lyophilized, for Solution by Apopharma USA, Inc.
  • 52609-4505 Deferoxamine Mesylate 500 mg Intramuscular; Intravenous; Subcutaneous Injection, Powder, Lyophilized, for Solution by Apopharma USA, Inc.
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  • 60505-6237 Deferoxamine Mesylate 2 g/1 Intramuscular; Intravenous Injection, Powder, Lyophilized, for Solution by Apotex Corp.
  • 60505-6238 Deferoxamine Mesylate 500 mg Intramuscular; Intravenous; Subcutaneous Injection, Powder, Lyophilized, for Solution by Apotex Corp.
  • 68083-172 Deferoxamine Mesylate 500 mg Intramuscular; Intravenous; Subcutaneous Injection, Powder, Lyophilized, for Solution by Gland Pharma Limited
  • 68083-173 Deferoxamine Mesylate 2 g/1 Intramuscular; Intravenous Injection, Powder, Lyophilized, for Solution by Gland Pharma Limited

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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.