Visitor Monitoring Drug History: REVIA
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: REVIA
FDA Application No: (NDA) 018932
Active Ingredient(s): NALTREXONE HYDROCHLORIDE
Company: DURAMED
 
Label History
 
Labels are not available on this site for REVIA, (NDA) 018932
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/15/2001 015Labeling Revision  
3/5/1999 014Labeling Revision  
3/5/1999 013Labeling Revision  
6/23/1995 012Formulation Revision  
12/30/1994 011Labeling Revision  
12/30/1994 010New or Modified Indication  
2/2/1989 007Control Supplement  
4/28/1987 005Control Supplement  
1/28/1986 003Labeling Revision  
2/8/1985 002Control Supplement  
11/30/1984 001Labeling Revision  
11/20/1984 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test