Visitor Monitoring Drug Details: CYTOVENE
 
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Drug Details

Drug Name: CYTOVENE
FDA Application No: (NDA) 020460
Active Ingredient(s): GANCICLOVIR
Company: ROCHE PALO
Original Approval or Tentative Approval Date: December 22, 1994
Chemical Type: 3 New dosage form
Review Classification: P Priority review drug
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
CYTOVENE GANCICLOVIR250MGCAPSULE; ORAL Discontinued No None
CYTOVENE GANCICLOVIR500MGCAPSULE; ORAL Discontinued No None


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