Visitor Monitoring Drug Details: FAMVIR
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: FAMVIR
FDA Application No: (NDA) 020363
Active Ingredient(s): FAMCICLOVIR
Company: NOVARTIS
Original Approval or Tentative Approval Date: June 29, 1994
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
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
FAMVIR FAMCICLOVIR250MGTABLET; ORAL Prescription No AB
FAMVIR FAMCICLOVIR500MGTABLET; ORAL Prescription Yes AB
FAMVIR FAMCICLOVIR125MGTABLET; ORAL Prescription No AB


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