Drug Details: DECADRON

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	DECADRON
FDA Application No:	(NDA) 011664
Active Ingredient(s):	DEXAMETHASONE
Company:	MERCK
Original Approval or Tentative Approval Date:	October 30, 1958
Chemical Type:	1 New molecular entity (NME)
Review Classification:	P Priority review drug

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
DECADRON	DEXAMETHASONE	0.5MG	TABLET; ORAL	Discontinued	No	None
DECADRON	DEXAMETHASONE	0.75MG	TABLET; ORAL	Discontinued	No	None
DECADRON	DEXAMETHASONE	1.5MG	TABLET; ORAL	Discontinued	No	None
DECADRON	DEXAMETHASONE	0.25MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET; ORAL	Discontinued	No	None
DECADRON	DEXAMETHASONE	4MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET; ORAL	Discontinued	No	None
DECADRON	DEXAMETHASONE	6MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET; ORAL	Discontinued	No	None

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