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Last Updated: August 14, 2024

NIPRIDE RTU IN SODIUM CHLORIDE 0.9% Drug Patent Profile


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When do Nipride Rtu In Sodium Chloride 0.9% patents expire, and what generic alternatives are available?

Nipride Rtu In Sodium Chloride 0.9% is a drug marketed by Exela Pharma and is included in one NDA.

The generic ingredient in NIPRIDE RTU IN SODIUM CHLORIDE 0.9% is sodium nitroprusside. There are one thousand four hundred and seventy-two drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the sodium nitroprusside profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Nipride Rtu In Sodium Chloride 0.9%

A generic version of NIPRIDE RTU IN SODIUM CHLORIDE 0.9% was approved as sodium nitroprusside by SAGENT PHARMS INC on December 8th, 2016.

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Summary for NIPRIDE RTU IN SODIUM CHLORIDE 0.9%
Drug patent expirations by year for NIPRIDE RTU IN SODIUM CHLORIDE 0.9%
Recent Clinical Trials for NIPRIDE RTU IN SODIUM CHLORIDE 0.9%

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SponsorPhase
University of AlbertaN/A
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)Phase 2
Curt TreuN/A

See all NIPRIDE RTU IN SODIUM CHLORIDE 0.9% clinical trials

Pharmacology for NIPRIDE RTU IN SODIUM CHLORIDE 0.9%
Drug ClassVasodilator
Physiological EffectVasodilation

US Patents and Regulatory Information for NIPRIDE RTU IN SODIUM CHLORIDE 0.9%

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Exela Pharma NIPRIDE RTU IN SODIUM CHLORIDE 0.9% sodium nitroprusside SOLUTION;INTRAVENOUS 209387-002 Dec 7, 2017 DISCN Yes No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Exela Pharma NIPRIDE RTU IN SODIUM CHLORIDE 0.9% sodium nitroprusside SOLUTION;INTRAVENOUS 209387-003 Jul 13, 2018 AP RX Yes Yes ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Exela Pharma NIPRIDE RTU IN SODIUM CHLORIDE 0.9% sodium nitroprusside SOLUTION;INTRAVENOUS 209387-001 Mar 8, 2017 AP RX Yes Yes ⤷  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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