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) 086009
Active Ingredient(s):
AMITRIPTYLINE HYDROCHLORIDE
Company:
MYLAN
Label History
Labels are not available on this site for AMITRIPTYLINE HYDROCHLORIDE, (ANDA) 086009
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/7/2002
049
Labeling
1/29/2001
048
Labeling
3/12/1999
047
Chemistry
3/12/1999
046
Chemistry
2/25/1998
045
Chemistry
2/5/1998
044
Chemistry
6/1/1995
043
Labeling
4/24/1995
042
Labeling
6/1/1995
041
Chemistry
6/1/1995
040
Chemistry
6/1/1995
039
Chemistry
11/24/1993
038
Chemistry
7/2/1993
037
Labeling in Effect
11/14/1991
035
Labeling
8/17/1989
034
SBA
8/17/1989
033
SBA
7/11/1989
032
Chemistry
7/11/1989
031
Chemistry
2/18/1988
027
Chemistry
7/2/1986
026
Chemistry
11/23/1984
024
Chemistry
6/15/1984
022
Chemistry
1/19/1983
021
Chemistry
1/19/1983
020
Chemistry
5/4/1982
017
Chemistry
4/10/1978
000
Approval
Therapeutic Equivalents
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