DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
IMODIUM
FDA Application No:
(NDA) 019037
Active Ingredient(s):
LOPERAMIDE HYDROCHLORIDE
Company:
JANSSEN PHARMA
Label History
Labels are not available on this site for IMODIUM, (NDA) 019037
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/16/1987
003
Labeling Revision
6/2/1986
002
Manufacturing Change or Addition
10/29/1985
001
Labeling Revision
7/31/1984
000
Approval
Therapeutic Equivalents
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