Drug Details: MAGNACORT

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	MAGNACORT
FDA Application No:	(NDA) 010554
Active Ingredient(s):	HYDROCORTAMATE HYDROCHLORIDE
Company:	PFIZER
Original Approval or Tentative Approval Date:	October 15, 1956
Chemical Type:	1 New molecular entity (NME)
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
MAGNACORT	HYDROCORTAMATE HYDROCHLORIDE	0.5%	OINTMENT; TOPICAL	Discontinued	No	None

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