Visitor Monitoring Drug History: KAYEXALATE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: KAYEXALATE
FDA Application No: (NDA) 011287
Active Ingredient(s): SODIUM POLYSTYRENE SULFONATE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for KAYEXALATE, (NDA) 011287
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/5/2003 018Labeling Revision Letter 
5/9/2003 017Labeling Revision Letter 
10/21/1991 016Labeling Revision  
10/25/1988 015Manufacturing Change or Addition  
8/25/1987 014Manufacturing Change or Addition  
9/24/1984 013Labeling Revision  
2/8/1985 012Package Change  
5/7/1991 011Practioner Draft Labeling  
8/6/1982 010Control Supplement  
7/17/1980 009Labeling Revision  
10/5/1979 008Distributor  
8/30/1977 007Labeling Revision  
8/22/1977 006Labeling Revision  
6/5/1958 000Approval  
 
There are no Therapeutic Equivalents
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