Drug Details: ZANTAC

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	ZANTAC
FDA Application No:	(NDA) 019675
Active Ingredient(s):	RANITIDINE HYDROCHLORIDE
Company:	GLAXOSMITHKLINE
Original Approval or Tentative Approval Date:	December 30, 1988
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

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
ZANTAC	RANITIDINE HYDROCHLORIDE	EQ 15MG BASE/ML	SYRUP; ORAL	Prescription	Yes	AA

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