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) 071562
Active Ingredient(s):
DOXEPIN HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for DOXEPIN HYDROCHLORIDE, (ANDA) 071562
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/9/2001
010
Control Supplement
3/13/1995
006
Labeling
3/1/1995
005
Chemistry
8/19/1993
004
Labeling in Effect
5/1/1991
003
Chemistry
1/17/1989
002
Labeling
9/1/1988
001
Labeling
3/2/1987
000
Approval
Therapeutic Equivalents
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