Drug Details: KENACORT

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	KENACORT
FDA Application No:	(NDA) 012515
Active Ingredient(s):	TRIAMCINOLONE DIACETATE
Company:	BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date:	March 21, 1961
Chemical Type:	5 New manufacturer
Review Classification:	S Standard review 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
KENACORT	TRIAMCINOLONE DIACETATE	EQ 4MG BASE/5ML	SYRUP; ORAL	Discontinued	No	None

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