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Last Updated: November 21, 2024

DEFEROXAMINE MESYLATE Drug Patent Profile


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When do Deferoxamine Mesylate patents expire, and when can generic versions of Deferoxamine Mesylate launch?

Deferoxamine Mesylate is a drug marketed by Dr Reddys, Fresenius Kabi Usa, Gland Pharma Ltd, Hospira, and West-ward Pharms Int. and is included in five NDAs.

The generic ingredient in DEFEROXAMINE MESYLATE is deferoxamine mesylate. There are seven drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the deferoxamine mesylate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Deferoxamine Mesylate

A generic version of DEFEROXAMINE MESYLATE was approved as deferoxamine mesylate by HOSPIRA on March 17th, 2004.

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Drug patent expirations by year for DEFEROXAMINE MESYLATE
Drug Prices for DEFEROXAMINE MESYLATE

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Recent Clinical Trials for DEFEROXAMINE MESYLATE

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SponsorPhase
Michigan Medicine PKUHSC Joint Institute for Translational & Clinical ResearchPhase 2
Aditya S. Pandey, MDPhase 2
People’s Hospital of Beijing Daxing DistrictPhase 1/Phase 2

See all DEFEROXAMINE MESYLATE clinical trials

Pharmacology for DEFEROXAMINE MESYLATE
Drug ClassIron Chelator
Mechanism of ActionIron Chelating Activity
Medical Subject Heading (MeSH) Categories for DEFEROXAMINE MESYLATE
Anatomical Therapeutic Chemical (ATC) Classes for DEFEROXAMINE MESYLATE

US Patents and Regulatory Information for DEFEROXAMINE MESYLATE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Dr Reddys DEFEROXAMINE MESYLATE deferoxamine mesylate INJECTABLE;INJECTION 076806-002 Mar 31, 2006 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Hospira DEFEROXAMINE MESYLATE deferoxamine mesylate INJECTABLE;INJECTION 076019-002 Mar 17, 2004 AP RX No Yes ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Fresenius Kabi Usa DEFEROXAMINE MESYLATE deferoxamine mesylate INJECTABLE;INJECTION 078718-001 Sep 15, 2009 AP RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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