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Last Updated: March 18, 2024

Mepivacaine hydrochloride - Generic Drug Details


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What are the generic sources for mepivacaine hydrochloride and what is the scope of freedom to operate?

Mepivacaine hydrochloride is the generic ingredient in seven branded drugs marketed by Solvay, Eastman Kodak, Hospira, Septodont, Belmora Llc, Hospira Inc, Intl Medication Sys, Watson Labs, Dentsply Pharm, Fresenius Kabi Usa, and Deproco, and is included in sixteen NDAs. Additional information is available in the individual branded drug profile pages.

There is one drug master file entry for mepivacaine hydrochloride. Twelve suppliers are listed for this compound.

Summary for mepivacaine hydrochloride
Recent Clinical Trials for mepivacaine hydrochloride

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

SponsorPhase
NorthShore University HealthSystemPhase 4
Johnny K. LeePhase 4
Research Institute of Ophthalmology, EgyptN/A

See all mepivacaine hydrochloride clinical trials

Pharmacology for mepivacaine hydrochloride
Drug ClassAmide Local Anesthetic
Physiological EffectLocal Anesthesia
Medical Subject Heading (MeSH) Categories for mepivacaine hydrochloride

US Patents and Regulatory Information for mepivacaine hydrochloride

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Fresenius Kabi Usa POLOCAINE-MPF mepivacaine hydrochloride INJECTABLE;INJECTION 089409-001 Dec 1, 1986 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Watson Labs MEPIVACAINE HYDROCHLORIDE mepivacaine hydrochloride INJECTABLE;INJECTION 088770-001 Nov 20, 1984 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Fresenius Kabi Usa POLOCAINE mepivacaine hydrochloride INJECTABLE;INJECTION 089407-001 Dec 1, 1986 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Hospira CARBOCAINE mepivacaine hydrochloride INJECTABLE;INJECTION 012250-005 Approved Prior to Jan 1, 1982 AP RX Yes Yes ⤷  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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