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) 071422
Active Ingredient(s):
DOXEPIN HYDROCHLORIDE
Company:
PAR PHARM
Label History
Labels are not available on this site for DOXEPIN HYDROCHLORIDE, (ANDA) 071422
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/31/2000
018
Labeling
11/26/1997
017
Chemistry
11/26/1997
016
Chemistry
11/21/1995
015
Labeling
8/25/1994
014
Chemistry
11/8/1993
013
Labeling in Effect
8/9/1994
012
Chemistry
6/28/1989
011
Labeling
4/3/1989
010
Labeling
3/15/1989
009
Labeling
5/12/1988
007
Labeling
4/19/1988
006
Labeling
3/30/1988
005
Labeling
3/30/1988
002
Chemistry
3/30/1988
001
Chemistry
11/9/1987
000
Approval
Therapeutic Equivalents
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