Visitor Monitoring Drug History: DOXEPIN HYDROCHLORIDE
 
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Label and Approval History

Drug Name: DOXEPIN HYDROCHLORIDE
FDA Application No: (NDA) 016987
Active Ingredient(s): DOXEPIN HYDROCHLORIDE
Company: NEW RIVER
 
Label History
 
Labels are not available on this site for DOXEPIN HYDROCHLORIDE, (NDA) 016987
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/19/1990 044Expiration Date Change  
10/13/1988 042Labeling Revision  
11/3/1987 039Package Change  
11/3/1987 038Package Change  
1/22/1988 037Labeling Revision  
11/6/1986 036Labeling Revision  
11/5/1987 035Expiration Date Change  
6/16/1986 034Expiration Date Change  
3/19/1986 033Package Change  
10/20/1986 032Package Change  
1/22/1985 031Labeling Revision  
11/21/1985 029Labeling Revision  
8/24/1984 028Expiration Date Change  
8/22/1984 027Control Supplement  
4/11/1984 026Labeling Revision  
3/29/1985 025Control Supplement  
9/19/1983 024Package Change  
9/19/1983 023Formulation Revision  
4/25/1983 022Control Supplement  
4/13/1987 018Formulation Revision  
4/15/1980 016Labeling Revision  
1/15/1980 015Formulation Revision  
6/8/1978 014Control Supplement  
9/15/1977 013Labeling Revision  
12/12/1977 011Control Supplement  
4/28/1975 010Efficacy (MarkIV)  
1/31/1972 000Approval  
 
Therapeutic Equivalents
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