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) 085969
Active Ingredient(s):
AMITRIPTYLINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for AMITRIPTYLINE HYDROCHLORIDE, (ANDA) 085969
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/16/2002
075
Control Supplement
6/25/2001
074
Labeling
3/23/2001
073
Control Supplement
8/7/2000
072
Labeling
5/5/1999
071
Chemistry
5/28/1998
070
Chemistry
11/18/1996
069
Chemistry
4/10/1995
068
Labeling
2/1/1995
067
Chemistry
8/27/1993
066
Labeling in Effect
12/15/1992
065
Labeling
7/17/1987
064
Chemistry
4/27/1987
063
Chemistry
7/17/1987
062
Chemistry
1/8/1987
061
Chemistry
1/8/1987
060
Chemistry
7/17/1987
059
Chemistry
7/17/1987
058
Chemistry
7/17/1987
057
Chemistry
7/17/1987
056
Chemistry
7/17/1987
055
Chemistry
1/8/1987
053
Chemistry
3/22/1985
049
Chemistry
1/25/1984
048
Chemistry
7/27/1983
046
Chemistry
7/27/1983
044
Chemistry
3/21/1983
043
Chemistry
3/21/1983
042
Chemistry
6/23/1982
041
Chemistry
6/23/1982
039
Chemistry
3/17/1982
037
Chemistry
3/17/1982
035
Chemistry
3/17/1982
033
Chemistry
3/17/1982
031
Chemistry
3/17/1982
030
Chemistry
3/17/1982
029
Chemistry
11/21/1977
000
Approval
Therapeutic Equivalents
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