VANCOCIN HYDROCHLORIDE Detail

Drug Name(s):
VANCOCIN HYDROCHLORIDE

FDA Application No.:
NDA 061667

Active Ingredient(s):
VANCOMYCIN HYDROCHLORIDE

Company:
VIROPHARMA

Original Approval or Tentative Approval Date:
July 12, 1983

Products on Application NDA 061667:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VANCOMYCIN HYDROCHLORIDE	EQ 500MG BASE/6ML	FOR SOLUTION; ORAL	Discontinued	none

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January 2009

VANCOCIN HYDROCHLORIDE Detail

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