Visitor Monitoring Drug History: AVENTYL HYDROCHLORIDE
 
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Label and Approval History

Drug Name: AVENTYL HYDROCHLORIDE
FDA Application No: (NDA) 014684
Active Ingredient(s): NORTRIPTYLINE HYDROCHLORIDE
Company: LILLY
 
Label History
 
Labels are not available on this site for AVENTYL HYDROCHLORIDE, (NDA) 014684
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/23/2000 040Labeling Revision  
5/29/1998 039Manufacturing Change or Addition  
6/19/1998 038Control Supplement  
4/3/1998 037Package Change  
8/23/2000 036Labeling Revision  
7/8/1996 035Labeling Revision  
6/16/1994 034Control Supplement  
7/8/1996 033Labeling Revision  
7/14/1993 032Control Supplement  
5/10/1993 031Labeling Revision  
5/22/1992 030Control Supplement  
5/10/1993 029Labeling Revision  
5/10/1993 028Labeling Revision  
6/20/1990 027Labeling Revision  
6/20/1990 026Labeling Revision  
4/19/1988 025Control Supplement  
4/7/1987 024Manufacturing Change or Addition  
6/10/1987 023Control Supplement  
6/15/1987 022Control Supplement  
6/20/1990 020Labeling Revision  
11/6/1985 019Labeling Revision  
10/5/1984 018Labeling Revision  
2/27/1984 017Labeling Revision  
7/19/1983 016Control Supplement  
3/18/1981 014Formulation Revision  
12/20/1979 013Formulation Revision  
7/7/1978 012Manufacturing Change or Addition  
6/1/1977 009Formulation Revision  
11/6/1964 000Approval Other Important Information from FDA 
 
Therapeutic Equivalents
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