Visitor Monitoring Drug History: MAPROTILINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: MAPROTILINE HYDROCHLORIDE
FDA Application No: (ANDA) 072164
Active Ingredient(s): MAPROTILINE HYDROCHLORIDE
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for MAPROTILINE HYDROCHLORIDE, (ANDA) 072164
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/7/2002 008Facility Addition  
11/10/1999 007Package Change  
8/26/1998 006Labeling  
6/4/1992 005Labeling in Effect  
5/20/1992 004Labeling  
11/29/1990 003Labeling in Effect  
5/15/1989 002Chemistry  
6/1/1988 000Approval  
 
Therapeutic Equivalents
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