DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
LANOXIN PEDIATRIC
FDA Application No:
(NDA) 009330
Active Ingredient(s):
DIGOXIN
Company:
GLAXOSMITHKLINE
Label History
Labels are not available on this site for LANOXIN PEDIATRIC, (NDA) 009330
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/17/2002
021
Manufacturing Change or Addition
Letter
7/15/1998
020
Labeling Revision
Review
6/25/1996
018
Labeling Revision
8/30/1995
017
Labeling Revision
8/6/1993
016
Control Supplement
5/7/1992
015
Labeling Revision
9/6/1991
014
Control Supplement
Therapeutic Equivalents
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