Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017820
Company: LILLY

Products on NDA 17820

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
DOBUTREX	DOBUTAMINE HYDROCHLORIDE	EQ 12.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	INJECTABLE;INJECTION	Discontinued	None	Yes	No