Drug Details: CERUBIDINE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	CERUBIDINE
FDA Application No:	(NDA) 050484
Active Ingredient(s):	DAUNORUBICIN HYDROCHLORIDE
Company:	WYETH AYERST
Original Approval or Tentative Approval Date:	December 19, 1979
Chemical Type:	1 New molecular entity (NME)
Review Classification:	P Priority review drug

Therapeutic Equivalents	Label Information
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
CERUBIDINE	DAUNORUBICIN HYDROCHLORIDE	EQ 20MG BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None

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