Drug Details: PROMETHAZINE HYDROCHLORIDE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	PROMETHAZINE HYDROCHLORIDE
FDA Application No:	(ANDA) 084555
Active Ingredient(s):	PROMETHAZINE HYDROCHLORIDE
Company:	MUTUAL PHARM
Original Approval or Tentative Approval Date:	July 29, 1976

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
PROMETHAZINE HYDROCHLORIDE	PROMETHAZINE HYDROCHLORIDE	12.5MG	TABLET; ORAL	Discontinued	No	None

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