VALTREX Detail

Drug Name(s):
VALTREX

FDA Application No.:
NDA 020487

Active Ingredient(s):
VALACYCLOVIR HYDROCHLORIDE

Company:
GLAXOSMITHKLINE

Original Approval or Tentative Approval Date:
June 22, 1995

Products on Application NDA 020487:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
VALACYCLOVIR HYDROCHLORIDE	EQ 1GM BASE	TABLET; ORAL	Prescription	none

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last updated on 11-21-2008

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