Drug Details: UNIPEN IN PLASTIC CONTAINER

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	UNIPEN IN PLASTIC CONTAINER
FDA Application No:	(NDA) 050320
Active Ingredient(s):	NAFCILLIN SODIUM
Company:	WYETH AYERST
Original Approval or Tentative Approval Date:	June 23, 1970

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
UNIPEN	NAFCILLIN SODIUM	EQ 2GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None
UNIPEN	NAFCILLIN SODIUM	EQ 4GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None
UNIPEN	NAFCILLIN SODIUM	EQ 10GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None
UNIPEN	NAFCILLIN SODIUM	EQ 20GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None
UNIPEN	NAFCILLIN SODIUM	EQ 500MG BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None
UNIPEN IN PLASTIC CONTAINER	NAFCILLIN SODIUM	EQ 1GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	No	None

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