Drug Details: BENZYL BENZOATE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	BENZYL BENZOATE
FDA Application No:	(ANDA) 084535
Active Ingredient(s):	BENZYL BENZOATE
Company:	LANNETT
Original Approval or Tentative Approval Date:	September 2, 1976

There are no 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
BENZYL BENZOATE	BENZYL BENZOATE	50%	EMULSION; TOPICAL	Discontinued	No	None

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