Drug Details: IMODIUM ADVANCED

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	IMODIUM ADVANCED
FDA Application No:	(NDA) 020606
Active Ingredient(s):	LOPERAMIDE HYDROCHLORIDE; SIMETHICONE
Company:	MCNEIL
Original Approval or Tentative Approval Date:	June 26, 1997
Chemical Type:	4 New combination
Review Classification:	S Standard review drug

There are no 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
IMODIUM ADVANCED	LOPERAMIDE HYDROCHLORIDE; SIMETHICONE	2MG; 125MG	TABLET, CHEWABLE; ORAL	OTC	Yes	None

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