VANCOLED Detail

Drug Name(s):
VANCOLED

FDA Application No.:
NDA 063321

Active Ingredient(s):
VANCOMYCIN HYDROCHLORIDE

Company:
LEDERLE

Original Approval or Tentative Approval Date:
August 3, 1995

Products on Application NDA 063321:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VANCOMYCIN HYDROCHLORIDE	EQ 250MG BASE/5ML	FOR SOLUTION; ORAL	Discontinued	none

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last updated on 12-01-2008

VANCOLED Detail

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