Visitor Monitoring Drug History: AMITRIPTYLINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: AMITRIPTYLINE HYDROCHLORIDE
FDA Application No: (ANDA) 085971
Active Ingredient(s): AMITRIPTYLINE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for AMITRIPTYLINE HYDROCHLORIDE, (ANDA) 085971
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/16/2002 064Control Supplement  
6/25/2001 063Labeling  
3/23/2001 062Control Supplement  
8/7/2000 061Labeling  
5/5/1999 060Chemistry  
5/28/1998 059Chemistry  
11/18/1996 058Chemistry  
4/10/1995 057Labeling  
2/1/1995 056Chemistry  
8/27/1993 055Labeling in Effect  
12/15/1992 054Labeling  
7/17/1987 053Chemistry  
4/27/1987 052Chemistry  
7/17/1987 051Chemistry  
1/8/1987 050Chemistry  
1/8/1987 049Chemistry  
7/17/1987 048Chemistry  
7/17/1987 047Chemistry  
7/17/1987 046Chemistry  
7/17/1987 045Chemistry  
7/17/1987 044Chemistry  
1/8/1987 043Chemistry  
3/22/1985 039Chemistry  
1/25/1984 038Chemistry  
7/27/1983 036Chemistry  
7/27/1983 034Chemistry  
7/27/1983 033Chemistry  
3/21/1983 032Chemistry  
6/23/1982 031Chemistry  
6/23/1982 029Chemistry  
11/29/1977 000Approval  
 
Therapeutic Equivalents
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