Visitor Monitoring Drug Details: VALTREX
 
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Drug Details

Drug Name: VALTREX
FDA Application No: (NDA) 020550
Active Ingredient(s): VALACYCLOVIR HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: December 15, 1995
Chemical Type: 6 New indication
Review Classification: P Priority review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
VALTREX VALACYCLOVIR HYDROCHLORIDEEQ 500MG BASETablet; Oral Prescription No None
VALTREX VALACYCLOVIR HYDROCHLORIDEEQ 1GM BASETABLET; ORAL Prescription No None


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