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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 072999

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NDA 072999 describes DOPAMINE HYDROCHLORIDE, which is a drug marketed by Abbott, Abraxis Pharm, Am Regent, Baxter Hlthcare, Hikma Intl Pharms, Hospira, Igi Labs Inc, Intl Medication, Lyphomed, Smith And Nephew, Teligent, Teva Parenteral, Warner Chilcott, and B Braun, and is included in thirty-six NDAs. It is available from six suppliers. Additional details are available on the DOPAMINE HYDROCHLORIDE profile page.

The generic ingredient in DOPAMINE HYDROCHLORIDE is dopamine hydrochloride. There are nine drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the dopamine hydrochloride profile page.

Summary for 072999

Tradename:	DOPAMINE HYDROCHLORIDE
Applicant:	Teva Parenteral
Ingredient:	dopamine hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 072999

Cardiotonic Agents
Dopamine Agents
Sympathomimetics

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	40MG/ML
Approval Date:	Oct 23, 1991	TE:		RLD:	No

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