DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
AMITRIPTYLINE HYDROCHLORIDE
FDA Application No:
(ANDA) 085966
Active Ingredient(s):
AMITRIPTYLINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for AMITRIPTYLINE HYDROCHLORIDE, (ANDA) 085966
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/16/2002
084
Control Supplement
6/25/2001
083
Labeling
3/23/2001
082
Control Supplement
8/7/2000
081
Labeling
10/5/1999
080
Chemistry
5/5/1999
079
Chemistry
5/28/1998
078
Chemistry
11/18/1996
077
Chemistry
4/17/1996
076
Chemistry
4/10/1995
075
Labeling
2/1/1995
074
Chemistry
8/27/1993
073
Labeling in Effect
12/15/1992
072
Labeling
7/17/1987
071
Chemistry
7/17/1987
070
Chemistry
7/17/1987
069
Chemistry
7/17/1987
068
Chemistry
7/17/1987
067
Chemistry
7/17/1987
066
Chemistry
7/17/1987
065
Chemistry
4/27/1987
064
Chemistry
1/8/1987
063
Chemistry
1/8/1987
062
Chemistry
1/8/1987
061
Chemistry
3/1/1985
054
Chemistry
3/1/1985
053
Chemistry
1/25/1984
052
Chemistry
7/27/1983
050
Chemistry
7/27/1983
048
Chemistry
7/27/1983
047
Chemistry
3/21/1983
046
Chemistry
7/23/1982
045
Chemistry
7/23/1982
043
Chemistry
2/2/1982
041
Chemistry
2/2/1982
040
Chemistry
3/21/1983
039
Chemistry
11/21/1977
000
Approval
Therapeutic Equivalents
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