BENZYL BENZOATE Detail

Drug Name(s):
BENZYL BENZOATE

FDA Application No.:
NDA 084535

Active Ingredient(s):
BENZYL BENZOATE

Company:
LANNETT

Original Approval or Tentative Approval Date:
September 1, 1976

Products on Application NDA 084535:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BENZYL BENZOATE	50%	EMULSION; TOPICAL	Discontinued	none

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last updated on 11-19-2008

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