Drug Details: LAMISIL

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	LAMISIL
FDA Application No:	(NDA) 020192
Active Ingredient(s):	TERBINAFINE HYDROCHLORIDE
Company:	NOVARTIS
Original Approval or Tentative Approval Date:	December 30, 1992
Chemical Type:	1 New molecular entity (NME)
Review Classification:	S Standard review drug

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
LAMISIL	TERBINAFINE HYDROCHLORIDE	1%	CREAM; TOPICAL	Discontinued	No	None

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