VANCOMYCIN HYDROCHLORIDE Detail

Drug Name(s):
VANCOMYCIN HYDROCHLORIDE

FDA Application No.:
NDA 062911

Active Ingredient(s):
VANCOMYCIN HYDROCHLORIDE

Company:
HOSPIRA

Original Approval or Tentative Approval Date:
August 3, 1988

Products on Application NDA 062911:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VANCOMYCIN HYDROCHLORIDE	EQ 500MG BASE/VIAL	INJECTABLE; INJECTION	Prescription	AP

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last updated on 12-01-2008