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) 071669
Active Ingredient(s):
DOXEPIN HYDROCHLORIDE
Company:
PAR PHARM
Label History
Labels are not available on this site for DOXEPIN HYDROCHLORIDE, (ANDA) 071669
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/31/2000
017
Labeling
11/26/1997
016
Chemistry
11/26/1997
015
Chemistry
11/21/1995
014
Labeling
8/25/1994
013
Chemistry
11/8/1993
012
Labeling in Effect
8/9/1994
011
Chemistry
6/28/1989
010
Labeling
4/3/1989
009
Labeling
3/15/1989
007
Labeling
3/15/1989
006
Chemistry
5/12/1988
005
Labeling
4/19/1988
004
Labeling
4/13/1988
003
Labeling
11/9/1987
000
Approval
Therapeutic Equivalents
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