Visitor Monitoring Drug History: MAPROTILINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: MAPROTILINE HYDROCHLORIDE
FDA Application No: (ANDA) 072284
Active Ingredient(s): MAPROTILINE HYDROCHLORIDE
Company: MYLAN
 
Label History
 
Labels are not available on this site for MAPROTILINE HYDROCHLORIDE, (ANDA) 072284
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/7/1998 011Chemistry  
2/26/1998 010Chemistry  
5/13/1998 009Labeling  
4/1/1996 008Labeling  
4/1/1996 007Chemistry  
9/27/1994 006Chemistry  
8/6/1993 005Labeling  
8/6/1993 004Chemistry  
8/4/1992 002Labeling  
1/31/1990 001Chemistry  
10/3/1988 000Approval  
 
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