Visitor Monitoring Drug History: SANOREX
 
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: SANOREX
FDA Application No: (NDA) 017247
Active Ingredient(s): MAZINDOL
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for SANOREX, (NDA) 017247
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/17/2001 042Manufacturing Change or Addition  
2/27/1996 041Manufacturing Change or Addition  
10/17/1995 040Control Supplement  
9/19/1994 038Control Supplement  
3/13/1995 037Control Supplement  
11/27/1992 036Labeling Revision  
8/2/1991 034Control Supplement  
3/29/1994 033Control Supplement  
3/14/1990 032Control Supplement  
9/14/1989 031Manufacturing Change or Addition  
11/18/1986 029Labeling Revision  
6/25/1981 027Manufacturing Change or Addition  
1/21/1981 026Package Change  
1/6/1982 025Labeling Revision  
1/16/1979 024Manufacturing Change or Addition  
3/23/1979 023Manufacturing Change or Addition  
9/19/1979 021Control Supplement  
6/28/1977 020Package Change  
9/20/1976 019Labeling Revision  
5/10/1976 018Package Change  
3/31/1976 017Package Change  
10/6/1975 014Control Supplement  
11/15/1974 012Control Supplement  
11/15/1974 011Labeling Revision  
11/15/1974 010Distributor  
6/14/1973 000Approval  
 
Therapeutic Equivalents
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