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Last Updated: November 21, 2024

CHLOROPROCAINE HYDROCHLORIDE Drug Patent Profile


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Which patents cover Chloroprocaine Hydrochloride, and when can generic versions of Chloroprocaine Hydrochloride launch?

Chloroprocaine Hydrochloride is a drug marketed by Hikma and Hospira and is included in three NDAs.

The generic ingredient in CHLOROPROCAINE HYDROCHLORIDE is chloroprocaine hydrochloride. There are four drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the chloroprocaine hydrochloride profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Chloroprocaine Hydrochloride

A generic version of CHLOROPROCAINE HYDROCHLORIDE was approved as chloroprocaine hydrochloride by HIKMA on September 9th, 1998.

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Drug patent expirations by year for CHLOROPROCAINE HYDROCHLORIDE
Recent Clinical Trials for CHLOROPROCAINE HYDROCHLORIDE

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SponsorPhase
Johns Hopkins UniversityPhase 3
Sintetica SAPhase 2/Phase 3
Sintetica SAPhase 1/Phase 2

See all CHLOROPROCAINE HYDROCHLORIDE clinical trials

Pharmacology for CHLOROPROCAINE HYDROCHLORIDE
Drug ClassEster Local Anesthetic
Physiological EffectLocal Anesthesia

US Patents and Regulatory Information for CHLOROPROCAINE HYDROCHLORIDE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Hikma CHLOROPROCAINE HYDROCHLORIDE chloroprocaine hydrochloride INJECTABLE;INJECTION 040273-001 Sep 9, 1998 AP RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Hospira CHLOROPROCAINE HYDROCHLORIDE chloroprocaine hydrochloride INJECTABLE;INJECTION 087446-001 Apr 16, 1982 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Hikma CHLOROPROCAINE HYDROCHLORIDE chloroprocaine hydrochloride INJECTABLE;INJECTION 040273-002 Sep 9, 1998 AP RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Hospira CHLOROPROCAINE HYDROCHLORIDE chloroprocaine hydrochloride INJECTABLE;INJECTION 087447-001 Apr 16, 1982 DISCN 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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