Visitor Monitoring Drug Details: KIONEX
 
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Drug Details

Drug Name: KIONEX
FDA Application No: (NDA) 040029
Active Ingredient(s): SODIUM POLYSTYRENE SULFONATE
Company: PADDOCK
Original Approval or Tentative Approval Date: February 6, 1998
 
 
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
KIONEX SODIUM POLYSTYRENE SULFONATE454GM/BOTPOWDER; ORAL, RECTAL Prescription No AA


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