DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
JANIMINE
FDA Application No:
(NDA) 017895
Active Ingredient(s):
IMIPRAMINE HYDROCHLORIDE
Company:
ABBOTT
Label History
Labels are not available on this site for JANIMINE, (NDA) 017895
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/12/1988
012
Control Supplement
12/14/1987
011
Expiration Date Change
12/13/1984
010
Labeling Revision
3/27/1984
009
Control Supplement
12/20/1983
008
Labeling Revision
7/15/1983
007
Manufacturing Change or Addition
6/25/1981
005
Expiration Date Change
4/8/1977
004
Labeling Revision
11/15/1974
000
Approval
Therapeutic Equivalents
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