Visitor Monitoring Drug History: NORTRIPTYLINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NORTRIPTYLINE HYDROCHLORIDE
FDA Application No: (ANDA) 073553
Active Ingredient(s): NORTRIPTYLINE HYDROCHLORIDE
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for NORTRIPTYLINE HYDROCHLORIDE, (ANDA) 073553
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/4/2002 019Labeling  
4/25/2001 018Control Supplement  
8/26/1998 016Chemistry  
8/26/1998 015Chemistry  
8/26/1998 014Chemistry  
8/26/1998 013Chemistry  
8/26/1998 012Chemistry  
2/7/1997 011Labeling  
12/5/1995 010Labeling  
5/25/1995 009Chemistry  
7/12/1995 008Chemistry  
5/25/1995 007Chemistry  
2/16/1995 006Chemistry  
2/16/1995 005Chemistry  
8/31/1993 004Labeling in Effect  
3/30/1992 000Approval  
 
Therapeutic Equivalents
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