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) 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 Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/19/2002
115
Control Supplement
5/9/2001
114
Control Supplement
10/16/2001
113
Control Supplement
10/31/2000
112
Control Supplement
5/11/1999
111
Labeling
5/5/1999
110
Chemistry
6/1/1999
108
Labeling
5/1/1999
107
Chemistry
3/21/1995
102
Labeling
4/6/1995
101
Chemistry
3/11/1994
100
Labeling
4/15/1991
099
Labeling in Effect
11/7/1989
098
Labeling in Effect
9/15/1989
097
Labeling
10/2/1990
096
Chemistry
6/30/1989
095
SBA
10/2/1990
095
Chemistry
2/22/1988
094
Chemistry
2/22/1988
093
Labeling
2/22/1988
092
Chemistry
2/22/1988
091
Chemistry
2/22/1988
090
Chemistry
2/22/1988
089
Chemistry
4/9/1987
087
Chemistry
7/30/1986
085
Chemistry
7/30/1986
082
Chemistry
7/30/1986
081
Chemistry
7/30/1986
080
Chemistry
1/16/1986
079
Chemistry
12/27/1985
078
Chemistry
10/21/1983
073
Chemistry
7/21/1983
071
Chemistry
12/10/1982
069
Chemistry
12/10/1982
068
Chemistry
6/9/1982
065
Chemistry
6/9/1982
064
Chemistry
4/20/1976
000
Approval
Therapeutic Equivalents
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