Drug Details: MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:	(NDA) 050581
Active Ingredient(s):	CEFOXITIN SODIUM
Company:	MERCK
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

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
MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER	CEFOXITIN SODIUM	EQ 20MG BASE/ML	INJECTABLE; INJECTION	Discontinued	No	None
MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER	CEFOXITIN SODIUM	EQ 40MG BASE/ML	INJECTABLE; INJECTION	Discontinued	No	None
MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	CEFOXITIN SODIUM	EQ 40MG BASE/ML	INJECTABLE; INJECTION	Discontinued	No	None
MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	CEFOXITIN SODIUM	EQ 20MG BASE/ML	INJECTABLE; INJECTION	Discontinued	No	None

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