Drug Details: KEFLIN

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	KEFLIN
FDA Application No:	(NDA) 050482
Active Ingredient(s):	CEPHALOTHIN SODIUM
Company:	LILLY
Original Approval or Tentative Approval Date:	December 18, 1974
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
KEFLIN	CEPHALOTHIN SODIUM	EQ 1GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None
KEFLIN	CEPHALOTHIN SODIUM	EQ 2GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None
KEFLIN	CEPHALOTHIN SODIUM	EQ 4GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None
KEFLIN	CEPHALOTHIN SODIUM	EQ 20GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None

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