Visitor Monitoring Drug History: IMIPRAMINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: IMIPRAMINE HYDROCHLORIDE
FDA Application No: (ANDA) 081049
Active Ingredient(s): IMIPRAMINE HYDROCHLORIDE
Company: MUTUAL PHARM
 
Label History
 
Labels are not available on this site for IMIPRAMINE HYDROCHLORIDE, (ANDA) 081049
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/6/2002 014Manufacturing Revision  
8/6/2002 013Control Supplement  
4/2/2001 012Control Supplement  
10/2/2000 011Labeling  
10/2/2000 010Packaging Addition  
5/16/2000 009Facility Addition  
5/16/2000 008Facility Addition  
5/26/1999 007Labeling  
12/5/1997 006Chemistry  
2/24/1997 005Chemistry  
11/9/1995 004Labeling  
6/22/1995 003Chemistry  
1/12/1994 002Chemistry  
7/30/1993 001Labeling  
6/5/1990 000Approval  
 
Therapeutic Equivalents
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