Visitor Monitoring Drug History: CANTIL
 
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: CANTIL
FDA Application No: (NDA) 010679
Active Ingredient(s): MEPENZOLATE BROMIDE
Company: SANOFI AVENTIS US
 
Label History
 
View the label approved on June 1, 2004 for CANTIL, (NDA) 010679


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/25/2004 029Labeling Revision Letter
Label 
1/29/1999 027Control Supplement  
1/11/1989 026Package Change  
7/15/1985 025Package Change  
11/9/1982 024Manufacturing Change or Addition  
5/8/1991 023Practioner Draft Labeling  
11/4/1980 021Labeling Revision  
11/9/1982 019Package Change  
6/20/1980 017Labeling Revision  
11/14/1956 000Approval  
 
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