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) 071918
Active Ingredient(s):
DOXEPIN HYDROCHLORIDE
Company:
MORTON GROVE
Label History
Labels are not available on this site for DOXEPIN HYDROCHLORIDE, (ANDA) 071918
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/5/2001
008
Labeling
1/11/2001
007
Labeling
8/17/1995
006
Labeling
8/17/1995
005
Labeling
11/24/1993
004
Labeling in Effect
2/12/1992
003
Labeling in Effect
4/2/1991
002
Labeling in Effect
7/20/1988
000
Approval
Therapeutic Equivalents
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