DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
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 Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/19/2002
109
Control Supplement
5/9/2001
108
Control Supplement
10/16/2001
107
Control Supplement
10/31/2000
106
Control Supplement
5/11/1999
105
Labeling
5/5/1999
104
Chemistry
6/1/1999
102
Labeling
6/1/1999
101
Chemistry
3/21/1995
096
Labeling
4/6/1995
095
Chemistry
3/11/1994
094
Labeling
5/15/1989
093
SBA
6/13/1991
092
Chemistry
6/13/1991
091
Chemistry
2/22/1988
090
Chemistry
2/22/1988
089
Chemistry
2/22/1988
087
Chemistry
2/22/1988
086
Chemistry
2/22/1988
085
Chemistry
5/29/1986
082
Chemistry
12/27/1985
080
Chemistry
3/11/1986
079
Chemistry
3/11/1986
078
Chemistry
3/11/1986
077
Chemistry
10/21/1983
072
Chemistry
7/25/1983
070
Chemistry
12/10/1982
067
Chemistry
4/7/1982
065
Chemistry
4/20/1976
000
Approval
Therapeutic Equivalents
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