DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DOXEPIN HYDROCHLORIDE
FDA Application No:
(ANDA) 071609
Active Ingredient(s):
DOXEPIN HYDROCHLORIDE
Company:
TEVA PHARMS
Label History
Labels are not available on this site for DOXEPIN HYDROCHLORIDE, (ANDA) 071609
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/13/2002
018
Labeling
2/27/2002
017
Facility Addition
2/27/2002
016
Formulation Revision
10/31/2001
015
Facility Addition
10/31/2001
014
Facility Addition
10/31/2001
013
Facility Addition
1/23/2002
012
Facility Addition
2/26/2001
011
Facility Addition
6/17/1999
010
Chemistry
3/23/1999
009
Chemistry
6/11/1998
008
Chemistry
11/13/1997
007
Chemistry
5/31/1996
006
Chemistry
7/12/1993
005
Labeling in Effect
5/27/1993
004
Chemistry
9/29/1992
003
Chemistry
9/29/1992
002
Chemistry
11/7/1990
001
Labeling
11/9/1987
000
Approval
Therapeutic Equivalents
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