Drug Details: NALLPEN IN PLASTIC CONTAINER

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	NALLPEN IN PLASTIC CONTAINER
FDA Application No:	(NDA) 050655
Active Ingredient(s):	NAFCILLIN SODIUM
Company:	BAXTER HLTHCARE
Original Approval or Tentative Approval Date:	October 31, 1989
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

There are no Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
NALLPEN IN PLASTIC CONTAINER	NAFCILLIN SODIUM	EQ 20MG BASE/ML	INJECTABLE; INJECTION	Prescription	Yes	None
NALLPEN IN PLASTIC CONTAINER	NAFCILLIN SODIUM	EQ 2GM BASE/100ML	INJECTABLE; INJECTION	Prescription	Yes	None

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