Drug Details: INDIUM IN-111 OXYQUINOLINE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	INDIUM IN-111 OXYQUINOLINE
FDA Application No:	(NDA) 019044
Active Ingredient(s):	INDIUM IN-111 OXYQUINOLINE
Company:	GE HEALTHCARE
Original Approval or Tentative Approval Date:	December 24, 1985
Chemical Type:	1 New molecular entity (NME)
Review Classification:	P Priority 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
INDIUM IN-111 OXYQUINOLINE	INDIUM IN-111 OXYQUINOLINE	1mCi/ML	INJECTABLE; INJECTION	Prescription	Yes	None

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