Drug Details: TAGAMET HB 200

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	TAGAMET HB 200
FDA Application No:	(NDA) 020951
Active Ingredient(s):	CIMETIDINE
Company:	GLAXOSMITHKLINE
Original Approval or Tentative Approval Date:	July 9, 1999
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

There are no Therapeutic Equivalents	Label Information
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
TAGAMET HB 200	CIMETIDINE	200MG/20ML	SUSPENSION; ORAL	Discontinued	No	None

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