DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
IMIPRAMINE HYDROCHLORIDE
FDA Application No:
(ANDA) 089497
Active Ingredient(s):
IMIPRAMINE HYDROCHLORIDE
Company:
PAR PHARM
Label History
Labels are not available on this site for IMIPRAMINE HYDROCHLORIDE, (ANDA) 089497
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/2/1997
012
Chemistry
3/25/1996
011
Chemistry
3/25/1996
010
Chemistry
3/25/1996
009
Labeling
10/23/1995
008
Labeling
11/5/1993
007
Labeling in Effect
1/7/1991
006
Labeling
8/16/1988
005
SBA
10/16/1995
005
Chemistry
8/19/1988
004
Chemistry
8/19/1988
003
Chemistry
8/19/1988
001
Chemistry
7/14/1987
000
Approval
Therapeutic Equivalents
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