Visitor Monitoring Drug History: NORTRIPTYLINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: NORTRIPTYLINE HYDROCHLORIDE
FDA Application No: (ANDA) 074132
Active Ingredient(s): NORTRIPTYLINE HYDROCHLORIDE
Company: TEVA
 
Label History
 
Labels are not available on this site for NORTRIPTYLINE HYDROCHLORIDE, (ANDA) 074132
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/20/2002 010Labeling  
8/30/2001 009Facility Addition  
7/7/2000 008Facility Addition  
7/21/1998 007Chemistry  
7/21/1998 006Chemistry  
3/27/1997 005Labeling  
1/25/1996 004Chemistry  
1/25/1996 003Chemistry  
1/25/1996 002Chemistry  
9/26/1995 001Labeling  
3/27/1995 000Approval  
 
Therapeutic Equivalents
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