Visitor Monitoring Drug History: SSD AF
 
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: SSD AF
FDA Application No: (NDA) 018578
Active Ingredient(s): SILVER SULFADIAZINE
Company: BASF
 
Label History
 
Labels are not available on this site for SSD AF, (NDA) 018578
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/24/2000 013Manufacturing Change or Addition  
1/12/1999 012Control Supplement  
1/11/1995 011Expiration Date Change  
8/3/1990 009Package Change  
7/11/1990 008Formulation Revision  
3/15/1989 007Manufacturing Change or Addition  
7/11/1990 006Labeling Revision  
12/10/1985 005Labeling Revision  
3/16/1984 004Package Change  
8/19/1983 003Labeling Revision  
5/12/1983 002Control Supplement  
1/29/1985 001Control Supplement  
2/25/1982 000Approval  
 
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