Drug Details: CORDARONE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	CORDARONE
FDA Application No:	(NDA) 020377
Active Ingredient(s):	AMIODARONE HYDROCHLORIDE
Company:	WYETH PHARMS INC
Original Approval or Tentative Approval Date:	August 3, 1995
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug
	O Orphan drug

There are no Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
CORDARONE	AMIODARONE HYDROCHLORIDE	50MG/ML	INJECTABLE; INJECTION	Discontinued	No	None

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