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) 084936
Active Ingredient(s):
IMIPRAMINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for IMIPRAMINE HYDROCHLORIDE, (ANDA) 084936
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/19/2002
097
Control Supplement
5/9/2001
096
Control Supplement
10/16/2001
095
Control Supplement
10/31/2000
094
Control Supplement
5/11/1999
093
Labeling
5/5/1999
092
Chemistry
3/21/1995
086
Labeling
4/6/1995
085
Chemistry
3/11/1994
084
Labeling
11/7/1989
083
Labeling in Effect
2/22/1988
082
Chemistry
1/19/1988
081
Chemistry
1/19/1988
080
Chemistry
1/19/1988
079
Chemistry
1/19/1988
078
Chemistry
1/19/1988
077
Chemistry
1/16/1986
073
Chemistry
12/27/1985
072
Chemistry
10/21/1983
066
Chemistry
7/19/1983
064
Chemistry
12/10/1982
062
Chemistry
6/9/1982
058
Chemistry
4/20/1976
000
Approval
Therapeutic Equivalents
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