Visitor Monitoring Drug Details: JANTOVEN
 
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Drug Details

Drug Name: JANTOVEN
FDA Application No: (NDA) 040416
Active Ingredient(s): WARFARIN SODIUM
Company: USL PHARMA
Original Approval or Tentative Approval Date: October 2, 2003
 
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
JANTOVEN WARFARIN SODIUM1MGTABLET; ORAL Prescription No AB
JANTOVEN WARFARIN SODIUM2MGTABLET; ORAL Prescription No AB
JANTOVEN WARFARIN SODIUM2.5MGTABLET; ORAL Prescription No AB
JANTOVEN WARFARIN SODIUM3MGTABLET; ORAL Prescription No AB
JANTOVEN WARFARIN SODIUM4MGTABLET; ORAL Prescription No AB
JANTOVEN WARFARIN SODIUM5MGTABLET; ORAL Prescription No AB
JANTOVEN WARFARIN SODIUM6MGTABLET; ORAL Prescription No AB
JANTOVEN WARFARIN SODIUM7.5MGTABLET; ORAL Prescription No AB
JANTOVEN WARFARIN SODIUM10MGTABLET; ORAL Prescription No AB


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