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Last Updated: March 28, 2024

FENOLDOPAM MESYLATE Drug Patent Profile


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Which patents cover Fenoldopam Mesylate, and when can generic versions of Fenoldopam Mesylate launch?

Fenoldopam Mesylate is a drug marketed by Hikma, Luitpold, Sandoz, and Teva Parenteral. and is included in four NDAs.

The generic ingredient in FENOLDOPAM MESYLATE is fenoldopam mesylate. There are five drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the fenoldopam mesylate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Fenoldopam Mesylate

A generic version of FENOLDOPAM MESYLATE was approved as fenoldopam mesylate by HIKMA on October 12th, 2004.

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Summary for FENOLDOPAM MESYLATE
Drug patent expirations by year for FENOLDOPAM MESYLATE
Recent Clinical Trials for FENOLDOPAM MESYLATE

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
University of Roma La SapienzaPhase 4
Southeast Renal Research InstitutePhase 4
Dialysis Clinic, Inc.Phase 2/Phase 3

See all FENOLDOPAM MESYLATE clinical trials

Medical Subject Heading (MeSH) Categories for FENOLDOPAM MESYLATE

US Patents and Regulatory Information for FENOLDOPAM MESYLATE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Hikma FENOLDOPAM MESYLATE fenoldopam mesylate INJECTABLE;INJECTION 076582-001 Oct 12, 2004 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Teva Parenteral FENOLDOPAM MESYLATE fenoldopam mesylate INJECTABLE;INJECTION 077826-001 Mar 7, 2007 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Luitpold FENOLDOPAM MESYLATE fenoldopam mesylate INJECTABLE;INJECTION 076656-001 Dec 1, 2003 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Sandoz FENOLDOPAM MESYLATE fenoldopam mesylate INJECTABLE;INJECTION 077155-001 Feb 15, 2005 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
>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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