Visitor Monitoring Drug History: BETADINE
 
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: BETADINE
FDA Application No: (NDA) 018634
Active Ingredient(s): POVIDONE-IODINE
Company: ALCON
 
Label History
 
Labels are not available on this site for BETADINE, (NDA) 018634
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/21/2003 007Labeling Revision Letter 
2/7/2000 006Manufacturing Change or Addition  
12/30/1991 004Labeling Revision  
12/30/1991 002Manufacturing Change or Addition  
10/27/1989 001Manufacturing Change or Addition  
12/17/1986 000Approval  
 
There are no Therapeutic Equivalents
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