VANCOCIN HYDROCHLORIDE Detail

Drug Name(s):
VANCOCIN HYDROCHLORIDE

FDA Application No.:
NDA 062716

Active Ingredient(s):
VANCOMYCIN HYDROCHLORIDE

Company:
VIROPHARMA

Original Approval or Tentative Approval Date:
July 21, 1987

Products on Application NDA 062716:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VANCOMYCIN HYDROCHLORIDE	EQ 500MG BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-01-2008