Visitor Monitoring Drug Details: PANWARFIN
 
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Drug Details

Drug Name: PANWARFIN
FDA Application No: (NDA) 017020
Active Ingredient(s): WARFARIN SODIUM
Company: ABBOTT
Original Approval or Tentative Approval Date: August 11, 1972
Chemical Type: 5 New manufacturer
Review Classification: S Standard 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
PANWARFIN WARFARIN SODIUM2MGTABLET; ORAL Discontinued No None
PANWARFIN WARFARIN SODIUM2.5MGTABLET; ORAL Discontinued No None
PANWARFIN WARFARIN SODIUM5MGTABLET; ORAL Discontinued No None
PANWARFIN WARFARIN SODIUM7.5MGTABLET; ORAL Discontinued No None
PANWARFIN WARFARIN SODIUM10MGTABLET; ORAL Discontinued No None


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