VANCOLED Detail

Drug Name(s):
VANCOLED

FDA Application No.:
NDA 062682

Active Ingredient(s):
VANCOMYCIN HYDROCHLORIDE

Company:
BAXTER HLTHCARE

Original Approval or Tentative Approval Date:
July 21, 1986

Products on Application NDA 062682:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VANCOMYCIN HYDROCHLORIDE	EQ 10GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none
VANCOMYCIN HYDROCHLORIDE	EQ 2GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none
VANCOMYCIN HYDROCHLORIDE	EQ 500MG BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-01-2008

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