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) 085200
Active Ingredient(s):
IMIPRAMINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for IMIPRAMINE HYDROCHLORIDE, (ANDA) 085200
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/20/1995
014
Labeling
6/25/1993
013
Labeling in Effect
3/12/1993
012
Labeling
7/31/1992
011
Labeling in Effect
4/26/1989
009
Labeling
2/22/1983
005
Chemistry
2/22/1983
004
Chemistry
8/22/1988
001
SBA
3/13/1981
000
Approval
Therapeutic Equivalents
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