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) 085133
Active Ingredient(s):
IMIPRAMINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for IMIPRAMINE HYDROCHLORIDE, (ANDA) 085133
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/20/1995
019
Labeling
3/12/1993
018
Labeling
6/25/1993
018
Labeling in Effect
7/31/1992
017
Labeling in Effect
4/26/1989
014
Labeling
9/11/1986
009
Chemistry
3/13/1981
000
Approval
Therapeutic Equivalents
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