Visitor Monitoring Drug History: IMIPRAMINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: IMIPRAMINE HYDROCHLORIDE
FDA Application No: (ANDA) 083745
Active Ingredient(s): IMIPRAMINE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for IMIPRAMINE HYDROCHLORIDE, (ANDA) 083745
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/19/2002 109Control Supplement  
5/9/2001 108Control Supplement  
10/16/2001 107Control Supplement  
10/31/2000 106Control Supplement  
5/11/1999 105Labeling  
5/5/1999 104Chemistry  
6/1/1999 102Labeling  
6/1/1999 101Chemistry  
3/21/1995 096Labeling  
4/6/1995 095Chemistry  
3/11/1994 094Labeling  
5/15/1989 093SBA  
6/13/1991 092Chemistry  
6/13/1991 091Chemistry  
2/22/1988 090Chemistry  
2/22/1988 089Chemistry  
2/22/1988 087Chemistry  
2/22/1988 086Chemistry  
2/22/1988 085Chemistry  
5/29/1986 082Chemistry  
12/27/1985 080Chemistry  
3/11/1986 079Chemistry  
3/11/1986 078Chemistry  
3/11/1986 077Chemistry  
10/21/1983 072Chemistry  
7/25/1983 070Chemistry  
12/10/1982 067Chemistry  
4/7/1982 065Chemistry  
4/20/1976 000Approval  
 
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