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Last Updated: November 22, 2024

LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE - Generic Drug Details


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What are the generic drug sources for levonordefrin; mepivacaine hydrochloride and what is the scope of patent protection?

Levonordefrin; mepivacaine hydrochloride is the generic ingredient in six branded drugs marketed by Solvay, Eastman Kodak, Septodont, Belmora Llc, Dentsply Pharm, and Deproco, and is included in six NDAs. Additional information is available in the individual branded drug profile pages.

Summary for LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE
US Patents:0
Tradenames:6
Applicants:6
NDAs:6
Clinical Trials: 4
DailyMed Link:LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE at DailyMed
Recent Clinical Trials for LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

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

SponsorPhase
Suez Canal UniversityN/A
Cairo UniversityN/A
University of Sao PauloN/A

See all LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE clinical trials

Anatomical Therapeutic Chemical (ATC) Classes for LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

US Patents and Regulatory Information for LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Belmora Llc MEPIVACAINE HYDROCHLORIDE W/ LEVONORDEFRIN levonordefrin; mepivacaine hydrochloride INJECTABLE;INJECTION 084850-002 Oct 21, 1983 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Deproco SCANDONEST L levonordefrin; mepivacaine hydrochloride INJECTABLE;INJECTION 088388-001 Oct 10, 1984 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Eastman Kodak CARBOCAINE W/ NEO-COBEFRIN levonordefrin; mepivacaine hydrochloride INJECTABLE;INJECTION 012125-002 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Septodont ISOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN levonordefrin; mepivacaine hydrochloride INJECTABLE;INJECTION 084697-001 Approved Prior to Jan 1, 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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