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Last Updated: November 24, 2024

AMINOPHYLLINE Drug Patent Profile


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

Aminophylline is a drug marketed by Abraxis Pharm, Am Regent, Elkins Sinn, Hospira, Intl Medication, King Pharms, Luitpold, Lyphomed, Pharma Serve Ny, Smith And Nephew, Teva Parenteral, Morton Grove, Roxane, Impax Labs, Tablicaps, Vale, Ani Pharms, Ascot, Barr, Chartwell Molecular, Duramed Pharms Barr, Halsey, Hikma Intl Pharms, Kv Pharm, Pal Pak, Panray, Purepac Pharm, Valeant Pharm Intl, Vangard, Vintage Pharms, Watson Labs, and Actavis Mid Atlantic. and is included in fifty-eight NDAs.

The generic ingredient in AMINOPHYLLINE is aminophylline. There are four drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the aminophylline profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Aminophylline

A generic version of AMINOPHYLLINE was approved as aminophylline by HOSPIRA on October 26th, 1983.

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Summary for AMINOPHYLLINE
Drug patent expirations by year for AMINOPHYLLINE
Recent Clinical Trials for AMINOPHYLLINE

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

SponsorPhase
Mahidol UniversityPhase 2/Phase 3
Medical College of WisconsinPhase 1/Phase 2
University of OklahomaPhase 1/Phase 2

See all AMINOPHYLLINE clinical trials

Pharmacology for AMINOPHYLLINE
Drug ClassMethylxanthine

US Patents and Regulatory Information for AMINOPHYLLINE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Impax Labs AMINOPHYLLINE aminophylline TABLET;ORAL 084574-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Barr AMINOPHYLLINE aminophylline TABLET;ORAL 088297-001 Aug 19, 1983 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Purepac Pharm AMINOPHYLLINE aminophylline TABLET;ORAL 085333-001 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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