Drug Details: CARDIOGEN-82

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	CARDIOGEN-82
FDA Application No:	(NDA) 019414
Active Ingredient(s):	RUBIDIUM CHLORIDE RB-82
Company:	BRACCO
Original Approval or Tentative Approval Date:	December 29, 1989
Chemical Type:	1 New molecular entity (NME)
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
CARDIOGEN-82	RUBIDIUM CHLORIDE RB-82	N/A	INJECTABLE; INJECTION	Prescription	No	None

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