Drug Details: HYTONE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	HYTONE
FDA Application No:	(ANDA) 080472
Active Ingredient(s):	HYDROCORTISONE
Company:	SANOFI AVENTIS US
Original Approval or Tentative Approval Date:	September 27, 1972

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
HYTONE	HYDROCORTISONE	1%	CREAM; TOPICAL	Prescription	Yes	AT
HYTONE	HYDROCORTISONE	2.5%	CREAM; TOPICAL	Prescription	Yes	AT

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