Visitor Monitoring Drug History: KLARON
 
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: KLARON
FDA Application No: (NDA) 019931
Active Ingredient(s): SULFACETAMIDE SODIUM
Company: SANOFI AVENTIS US
 
Label History
 
View the label approved on June 7, 2004 for KLARON, (NDA) 019931


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/21/2003 008Control Supplement Letter
Label 
10/9/2002 007Manufacturing Change or Addition  
10/9/2002 006Manufacturing Change or Addition  
9/12/2002 005Manufacturing Change or Addition  
9/12/2002 004Manufacturing Change or Addition  
3/26/2002 003Manufacturing Change or Addition  
6/15/1999 001Manufacturing Change or Addition  
12/23/1996 000Approval Review 
 
Therapeutic Equivalents
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