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) 071239
Active Ingredient(s):
DOXEPIN HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for DOXEPIN HYDROCHLORIDE, (ANDA) 071239
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/25/2001
015
Control Supplement
12/15/2000
014
Labeling
12/15/1997
012
Chemistry
12/19/1995
011
Labeling
8/27/1993
010
Labeling in Effect
5/22/1991
009
Labeling
11/19/1990
008
Chemistry
5/31/1991
007
Chemistry
6/29/1990
006
Chemistry
6/3/1988
005
Chemistry
6/3/1988
004
Chemistry
11/6/1987
002
Chemistry
11/6/1987
001
Chemistry
4/30/1987
000
Approval
Therapeutic Equivalents
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