Visitor Monitoring Drug History: SEPTRA
 
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: SEPTRA
FDA Application No: (NDA) 018452
Active Ingredient(s): SULFAMETHOXAZOLE; TRIMETHOPRIM
Company: MONARCH PHARMS
 
Label History
 
Labels are not available on this site for SEPTRA, (NDA) 018452
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/14/1997 024Labeling Revision  
7/12/1996 023Manufacturing Change or Addition  
3/19/1997 022Labeling Revision  
9/11/1996 021Labeling Revision  
3/16/1993 020Manufacturing Change or Addition  
2/22/1993 019Manufacturing Change or Addition  
8/21/1992 018Labeling Revision  
12/1/1992 017Control Supplement  
3/19/1997 016Labeling Revision  
7/9/1990 015Package Change  
4/6/1989 014Control Supplement  
3/19/1997 013Labeling Revision  
3/19/1997 012Labeling Revision  
11/2/1987 010Manufacturing Change or Addition  
4/22/1987 009Control Supplement  
11/9/1990 008Labeling Revision  
8/11/1987 007Labeling Revision  
3/14/1986 006Manufacturing Change or Addition  
6/1/1984 005Labeling Revision  
5/16/1983 004Package Change  
11/1/1984 002Practioner Draft Labeling  
9/16/1982 001Control Supplement  
6/23/1981 000Approval  
 
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