Visitor Monitoring Drug History: ELAVIL
 
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: ELAVIL
FDA Application No: (NDA) 012703
Active Ingredient(s): AMITRIPTYLINE HYDROCHLORIDE
Company: ASTRAZENECA
 
Label History
 
Labels are not available on this site for ELAVIL, (NDA) 012703
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/29/2003 093Labeling Revision Letter 
3/27/2001 092Labeling Revision Letter 
1/22/2001 091Control Supplement  
4/5/2000 090Labeling Revision  
12/24/1998 089Manufacturing Change or Addition  
4/5/2000 088Labeling Revision  
12/30/1996 087Package Change  
4/5/2000 086Labeling Revision  
7/13/1995 085Control Supplement  
4/5/2000 084Labeling Revision  
6/1/1994 083Formulation Revision  
6/1/1994 082Control Supplement  
6/24/1991 081Labeling Revision  
7/28/1989 080Manufacturing Change or Addition  
6/24/1991 079Labeling Revision  
4/8/1988 078Package Change  
12/12/1988 077Formulation Revision  
6/24/1991 076Labeling Revision  
2/26/1988 075Control Supplement  
4/2/1986 074Expiration Date Change  
7/10/1986 073Labeling Revision  
9/20/1985 072Labeling Revision  
9/13/1984 071Package Change  
8/15/1984 070Package Change  
3/7/1984 069Manufacturing Change or Addition  
3/15/1983 068Labeling Revision  
5/26/1983 067Manufacturing Change or Addition  
5/21/1984 065Labeling Revision  
5/3/1983 064Control Supplement  
6/25/1981 062Manufacturing Change or Addition  
3/23/1981 061Labeling Revision  
9/3/1980 060Labeling Revision  
6/23/1980 059Labeling Revision  
3/2/1981 058Formulation Revision  
9/4/1981 057Formulation Revision  
3/2/1981 056Manufacturing Change or Addition  
3/4/1980 054Labeling Revision  
1/29/1980 053Labeling Revision  
11/6/1979 052Labeling Revision  
3/2/1981 050Manufacturing Change or Addition  
1/29/1980 049Manufacturing Change or Addition  
1/25/1978 046Package Change  
3/1/1977 044Package Change  
8/2/1976 043Control Supplement  
9/17/1976 042Labeling Revision  
8/2/1976 041Control Supplement  
10/28/1976 039Labeling Revision  
9/18/1975 038Labeling Revision  
9/18/1975 037Labeling Revision  
9/17/1975 036Control Supplement  
9/17/1975 035Control Supplement  
3/9/1981 032Control Supplement  
4/7/1961 000Approval Other Important Information from FDA 
 
©2019 Drugs That Causes a False Positive on a Drug Test