Visitor Monitoring Drug History: BENDECTIN
 
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: BENDECTIN
FDA Application No: (NDA) 010598
Active Ingredient(s): DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for BENDECTIN, (NDA) 010598
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/9/1982 014Package Change  
9/7/1982 013Labeling Revision  
6/16/1982 012Control Supplement  
10/22/1981 011Labeling Revision  
10/22/1981 010Labeling Revision  
1/9/1981 009Labeling Revision  
11/6/1979 008Formulation Revision  
7/25/1979 007Manufacturing Change or Addition  
11/1/1978 006Expiration Date Change  
8/1/1978 005Labeling Revision  
11/9/1976 003Labeling Revision  
11/9/1976 002General Efficacy (MarkIV)  
7/30/1956 000Approval  
 
There are no Therapeutic Equivalents
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