Last Updated: May 5, 2026

DOBUTAMINE HYDROCHLORIDE Drug Patent Profile


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Which patents cover Dobutamine Hydrochloride, and what generic alternatives are available?

Dobutamine Hydrochloride is a drug marketed by Baxter Hlthcare, Dr Reddys, Hikma, Hospira, Luitpold, Slate Run Pharma, Teligent, Teva Parenteral, Watson Labs, and Watson Labs Inc. and is included in fifteen NDAs.

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

DrugPatentWatch® Litigation and Generic Entry Outlook for Dobutamine Hydrochloride

A generic version of DOBUTAMINE HYDROCHLORIDE was approved as dobutamine hydrochloride by HOSPIRA on November 29th, 1993.

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Summary for DOBUTAMINE HYDROCHLORIDE
US Patents:0
Applicants:10
NDAs:15

US Patents and Regulatory Information for DOBUTAMINE HYDROCHLORIDE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Baxter Hlthcare DOBUTAMINE HYDROCHLORIDE dobutamine hydrochloride INJECTABLE;INJECTION 074381-001 Sep 26, 1996 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Baxter Hlthcare DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER dobutamine hydrochloride INJECTABLE;INJECTION 020255-004 Oct 19, 1993 AP RX Yes Yes ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Luitpold DOBUTAMINE HYDROCHLORIDE dobutamine hydrochloride INJECTABLE;INJECTION 074545-001 Jun 25, 1998 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Hospira DOBUTAMINE HYDROCHLORIDE dobutamine hydrochloride INJECTABLE;INJECTION 074634-001 Sep 27, 1996 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Watson Labs Inc DOBUTAMINE HYDROCHLORIDE dobutamine hydrochloride INJECTABLE;INJECTION 074279-001 Feb 18, 1998 DISCN 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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