Last Updated: June 22, 2026

LEVALBUTEROL Drug Patent Profile


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

Levalbuterol is a drug marketed by Cipla, Impax Labs Inc, Luoxin Aurovitas, Mankind Pharma, Mylan Speciality Lp, Pharmobedient, Ritedose Corp, Sun Pharm, Teva Parenteral, and Teva Pharms Usa. and is included in eleven NDAs.

The generic ingredient in LEVALBUTEROL is levalbuterol hydrochloride. There are nine drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the levalbuterol hydrochloride profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Levalbuterol

A generic version of LEVALBUTEROL was approved as levalbuterol hydrochloride by IMPAX LABS INC on April 9th, 2008.

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Summary for LEVALBUTEROL
US Patents:0
Applicants:10
NDAs:11
Drug Prices: Drug price information for LEVALBUTEROL
DailyMed Link:LEVALBUTEROL at DailyMed

US Patents and Regulatory Information for LEVALBUTEROL

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Cipla LEVALBUTEROL HYDROCHLORIDE levalbuterol hydrochloride SOLUTION;INHALATION 078171-002 Dec 13, 2013 AN RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Ritedose Corp LEVALBUTEROL HYDROCHLORIDE levalbuterol hydrochloride SOLUTION;INHALATION 203653-001 Mar 22, 2016 AN RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Teva Parenteral LEVALBUTEROL HYDROCHLORIDE levalbuterol hydrochloride SOLUTION;INHALATION 200875-001 Sep 11, 2014 AN RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Luoxin Aurovitas LEVALBUTEROL HYDROCHLORIDE levalbuterol hydrochloride SOLUTION;INHALATION 207628-001 Jan 31, 2017 AN RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Impax Labs Inc LEVALBUTEROL HYDROCHLORIDE levalbuterol hydrochloride SOLUTION;INHALATION 077756-003 Apr 9, 2008 AN RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start 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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