BENZAMYCIN PAK Detail

Drug Name(s):
BENZAMYCIN PAK

FDA Application No.:
NDA 050769

Active Ingredient(s):
BENZOYL PEROXIDE; ERYTHROMYCIN

Company:
SANOFI AVENTIS US

Original Approval or Tentative Approval Date:
November 26, 2000

Products on Application NDA 050769:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
BENZOYL PEROXIDE; ERYTHROMYCIN	5%;3%	GEL; TOPICAL	Prescription	none

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January 2009

BENZAMYCIN PAK Detail

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