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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 074206

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NDA 074206 describes DOBUTAMINE HYDROCHLORIDE, which 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. It is available from five suppliers. Additional details are available on the DOBUTAMINE HYDROCHLORIDE profile page.

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.

Summary for 074206

Tradename:	DOBUTAMINE HYDROCHLORIDE
Applicant:	Teva Parenteral
Ingredient:	dobutamine hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 074206

Adrenergic beta-1 Receptor Agonists
Cardiotonic Agents
Sympathomimetics

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	EQ 12.5MG BASE/ML
Approval Date:	Oct 19, 1993	TE:		RLD:	No

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