Visitor Monitoring Drug History: SANSERT
 
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: SANSERT
FDA Application No: (NDA) 012516
Active Ingredient(s): METHYSERGIDE MALEATE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for SANSERT, (NDA) 012516
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/3/2001 050Manufacturing Change or Addition  
5/10/2001 049Manufacturing Change or Addition  
3/16/2000 048Manufacturing Change or Addition  
4/21/1999 047Package Change  
10/15/1999 046Labeling Revision  
12/11/2000 045Labeling Revision  
3/20/1996 044Control Supplement  
11/22/1995 043Manufacturing Change or Addition  
10/17/1995 042Control Supplement  
12/11/2000 041Labeling Revision  
10/15/1999 040Labeling Revision  
12/11/2000 038Labeling Revision  
8/10/1981 026Manufacturing Change or Addition  
8/10/1981 025Formulation Revision  
10/11/1978 024Package Change  
3/20/1978 022Package Change  
5/7/1976 021Manufacturing Change or Addition  
1/29/1976 019Control Supplement  
8/12/1975 018Control Supplement  
1/6/1975 017Control Supplement  
8/26/1974 016Labeling Revision  
7/3/1974 015Control Supplement  
2/12/1962 000Approval  
 
There are no Therapeutic Equivalents
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