Visitor Monitoring Drug History: DOXEPIN HYDROCHLORIDE
 
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Label and Approval History

Drug Name: DOXEPIN HYDROCHLORIDE
FDA Application No: (ANDA) 071609
Active Ingredient(s): DOXEPIN HYDROCHLORIDE
Company: TEVA PHARMS
 
Label History
 
Labels are not available on this site for DOXEPIN HYDROCHLORIDE, (ANDA) 071609
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/13/2002 018Labeling  
2/27/2002 017Facility Addition  
2/27/2002 016Formulation Revision  
10/31/2001 015Facility Addition  
10/31/2001 014Facility Addition  
10/31/2001 013Facility Addition  
1/23/2002 012Facility Addition  
2/26/2001 011Facility Addition  
6/17/1999 010Chemistry  
3/23/1999 009Chemistry  
6/11/1998 008Chemistry  
11/13/1997 007Chemistry  
5/31/1996 006Chemistry  
7/12/1993 005Labeling in Effect  
5/27/1993 004Chemistry  
9/29/1992 003Chemistry  
9/29/1992 002Chemistry  
11/7/1990 001Labeling  
11/9/1987 000Approval  
 
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