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) 085967
Active Ingredient(s):
AMITRIPTYLINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for AMITRIPTYLINE HYDROCHLORIDE, (ANDA) 085967
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/16/2002
066
Control Supplement
6/25/2001
065
Labeling
3/23/2001
064
Control Supplement
8/7/2000
063
Labeling
5/5/1999
062
Chemistry
5/28/1998
061
Chemistry
11/18/1996
060
Chemistry
11/20/1995
059
Chemistry
4/10/1995
058
Labeling
2/1/1995
057
Chemistry
8/27/1993
056
Labeling in Effect
12/15/1992
055
Labeling
7/17/1987
054
Chemistry
4/27/1987
053
Chemistry
4/27/1987
052
Chemistry
4/27/1987
051
Chemistry
4/27/1987
050
Chemistry
7/17/1987
049
Chemistry
7/17/1987
048
Chemistry
7/17/1987
047
Chemistry
7/17/1987
046
Chemistry
7/17/1987
045
Chemistry
7/17/1987
044
Chemistry
3/12/1985
037
Chemistry
1/25/1984
036
Chemistry
7/27/1983
034
Chemistry
7/27/1983
032
Chemistry
7/27/1983
031
Chemistry
3/21/1983
030
Chemistry
6/23/1982
029
Chemistry
6/23/1982
027
Chemistry
2/2/1982
025
Chemistry
2/2/1982
024
Chemistry
11/21/1977
000
Approval
Therapeutic Equivalents
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