Drug Details: HYDROCORTONE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	HYDROCORTONE
FDA Application No:	(NDA) 012052
Active Ingredient(s):	HYDROCORTISONE SODIUM PHOSPHATE
Company:	MERCK
Original Approval or Tentative Approval Date:	June 8, 1960
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

Therapeutic Equivalents	Labels are not available
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
HYDROCORTONE	HYDROCORTISONE SODIUM PHOSPHATE	EQ 50MG BASE/ML	INJECTABLE; INJECTION	Discontinued	No	None

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