Visitor Monitoring Drug History: NALFON
 
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: NALFON
FDA Application No: (NDA) 017710
Active Ingredient(s): FENOPROFEN CALCIUM
Company: DISTA
 
Label History
 
Labels are not available on this site for NALFON, (NDA) 017710
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/22/1997 026Control Supplement  
4/25/1994 023Manufacturing Change or Addition  
3/29/1995 021Labeling Revision  
7/8/1987 015Manufacturing Change or Addition  
3/4/1988 014Control Supplement  
2/8/1988 013Manufacturing Change or Addition  
6/9/1986 012Labeling Revision  
7/8/1987 011Control Supplement  
3/31/1983 010Labeling Revision  
12/11/1987 009Control Supplement  
8/9/1983 007Labeling Revision  
2/10/1982 006Package Change  
2/10/1982 005Package Change  
8/9/1983 004Labeling Revision  
4/9/1980 003Formulation Revision  
6/9/1977 000Approval  
 
Therapeutic Equivalents
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