DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FURADANTIN
FDA Application No:
(NDA) 008693
Active Ingredient(s):
NITROFURANTOIN
Company:
PROCTER AND GAMBLE
Label History
Labels are not available on this site for FURADANTIN, (NDA) 008693
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/16/1997
030
Labeling Revision
3/27/1997
029
Labeling Revision
2/17/1998
028
Labeling Revision
8/9/1993
027
Control Supplement
2/17/1998
026
Labeling Revision
5/13/1988
025
Labeling Revision
Review
7/14/1983
021
Manufacturing Change or Addition
5/18/1993
020
New or Modified Indication
11/18/1982
019
Labeling Revision
6/29/1979
017
Manufacturing Change or Addition
12/17/1979
016
Labeling Revision
3/16/1979
015
Package Change
5/11/1976
011
Manufacturing Change or Addition
6/30/1976
010
Manufacturing Change or Addition
2/6/1953
000
Approval
Therapeutic Equivalents
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