Drug Details: ZYVOX

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	ZYVOX
FDA Application No:	(NDA) 021130
Active Ingredient(s):	LINEZOLID
Company:	PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date:	April 18, 2000
Chemical Type:	1 New molecular entity (NME)
Review Classification:	P Priority review drug

There are no Therapeutic Equivalents	Label Information
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
ZYVOX	LINEZOLID	400MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET; ORAL	Discontinued	No	None
ZYVOX	LINEZOLID	600MG	TABLET; ORAL	Prescription	Yes	None

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