Visitor Monitoring Drug History: IMIPRAMINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: IMIPRAMINE HYDROCHLORIDE
FDA Application No: (ANDA) 084937
Active Ingredient(s): IMIPRAMINE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for IMIPRAMINE HYDROCHLORIDE, (ANDA) 084937
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/19/2002 115Control Supplement  
5/9/2001 114Control Supplement  
10/16/2001 113Control Supplement  
10/31/2000 112Control Supplement  
5/11/1999 111Labeling  
5/5/1999 110Chemistry  
6/1/1999 108Labeling  
5/1/1999 107Chemistry  
3/21/1995 102Labeling  
4/6/1995 101Chemistry  
3/11/1994 100Labeling  
4/15/1991 099Labeling in Effect  
11/7/1989 098Labeling in Effect  
9/15/1989 097Labeling  
10/2/1990 096Chemistry  
6/30/1989 095SBA  
10/2/1990 095Chemistry  
2/22/1988 094Chemistry  
2/22/1988 093Labeling  
2/22/1988 092Chemistry  
2/22/1988 091Chemistry  
2/22/1988 090Chemistry  
2/22/1988 089Chemistry  
4/9/1987 087Chemistry  
7/30/1986 085Chemistry  
7/30/1986 082Chemistry  
7/30/1986 081Chemistry  
7/30/1986 080Chemistry  
1/16/1986 079Chemistry  
12/27/1985 078Chemistry  
10/21/1983 073Chemistry  
7/21/1983 071Chemistry  
12/10/1982 069Chemistry  
12/10/1982 068Chemistry  
6/9/1982 065Chemistry  
6/9/1982 064Chemistry  
4/20/1976 000Approval  
 
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