DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FUROSEMIDE
FDA Application No:
(NDA) 018487
Active Ingredient(s):
FUROSEMIDE
Company:
MYLAN
Label History
Labels are not available on this site for FUROSEMIDE, (NDA) 018487
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/25/2001
032
Control Supplement
9/25/2001
031
Facility Addition
12/7/1998
030
Chemistry
2/25/1998
029
Chemistry
2/5/1998
028
Chemistry
10/6/1997
027
Labeling
4/29/1996
026
Labeling
1/7/1994
025
Chemistry
6/15/1993
024
Labeling
4/13/1993
022
Labeling
5/6/1992
021
Labeling
3/18/1992
020
Labeling
12/27/1990
019
Labeling
7/5/1990
018
Labeling
9/19/1989
017
SBA
1/31/1990
017
Chemistry
9/19/1989
016
Chemistry
3/1/1988
015
Chemistry
3/1/1988
014
Chemistry
10/13/1989
013
Labeling
1/9/1985
007
Chemistry
8/27/1981
000
Approval
Therapeutic Equivalents
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