VANCOCIN HYDROCHLORIDE Detail

Drug Name(s):
VANCOCIN HYDROCHLORIDE

FDA Application No.:
NDA 062812

Active Ingredient(s):
VANCOMYCIN HYDROCHLORIDE

Company:
VIROPHARMA

Original Approval or Tentative Approval Date:
November 2, 1992

Products on Application NDA 062812:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VANCOMYCIN HYDROCHLORIDE	EQ 1GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-01-2008