Visitor Monitoring Drug History: DIDREX
 
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: DIDREX
FDA Application No: (NDA) 012427
Active Ingredient(s): BENZPHETAMINE HYDROCHLORIDE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for DIDREX, (NDA) 012427
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/23/1998 023Package Change  
7/31/1992 022Control Supplement  
7/28/2000 021Labeling Revision  
7/27/2000 020Labeling Revision  
12/31/1985 019Labeling Revision  
9/4/1984 018Labeling Revision  
10/26/1960 000Approval  
 
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