Visitor Monitoring Drug History: TOFRANIL
 
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Label and Approval History

Drug Name: TOFRANIL
FDA Application No: (NDA) 011838
Active Ingredient(s): IMIPRAMINE HYDROCHLORIDE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for TOFRANIL, (NDA) 011838
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/17/1998 034Manufacturing Change or Addition  
12/8/1992 032Labeling Revision  
12/24/1992 031Control Supplement  
11/27/1985 029Control Supplement  
5/13/1985 028Control Supplement  
4/29/1985 027Labeling Revision  
10/30/1984 026Labeling Revision  
5/1/1984 025Labeling Revision  
6/7/1983 023Manufacturing Change or Addition  
3/20/1981 022Control Supplement  
3/31/1980 021Manufacturing Change or Addition  
12/1/1978 020Labeling Revision  
10/2/1959 000Approval Other Important Information from FDA 
 
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