Visitor Monitoring Drug Details: WARFARIN SODIUM
 
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Drug Details

Drug Name: WARFARIN SODIUM
FDA Application No: (NDA) 040663
Active Ingredient(s): WARFARIN SODIUM
Company: ZYDUS PHARMS USA
Original Approval or Tentative Approval Date: May 30, 2006
 
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
WARFARIN SODIUM WARFARIN SODIUM1MGTABLET; ORAL Prescription No AB
WARFARIN SODIUM WARFARIN SODIUM2MGTABLET; ORAL Prescription No AB
WARFARIN SODIUM WARFARIN SODIUM2.5MGTABLET; ORAL Prescription No AB
WARFARIN SODIUM WARFARIN SODIUM3MGTABLET; ORAL Prescription No AB
WARFARIN SODIUM WARFARIN SODIUM4MGTABLET; ORAL Prescription No AB
WARFARIN SODIUM WARFARIN SODIUM5MGTABLET; ORAL Prescription No AB
WARFARIN SODIUM WARFARIN SODIUM6MGTABLET; ORAL Prescription No AB
WARFARIN SODIUM WARFARIN SODIUM7.5MGTABLET; ORAL Prescription No AB
WARFARIN SODIUM WARFARIN SODIUM10MGTABLET; ORAL Prescription No AB


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