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) 018569
Active Ingredient(s):
FUROSEMIDE
Company:
SANDOZ
Label History
Labels are not available on this site for FUROSEMIDE, (NDA) 018569
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/16/2002
052
Control Supplement
4/19/2002
051
Control Supplement
6/14/2001
050
Control Supplement
6/14/2001
049
Package Change
11/20/2000
048
Supplier Addition
2/3/2000
047
Control Supplement
5/5/1999
045
Chemistry
9/15/1997
044
Chemistry
11/8/1996
043
Chemistry
2/8/1995
042
Chemistry
4/13/1994
041
Chemistry
3/30/1993
040
Labeling
7/24/1992
039
Labeling
10/19/1989
038
Labeling in Effect
5/17/1989
037
Labeling
8/25/1988
036
Labeling
12/6/1988
034
Chemistry
12/6/1988
033
Chemistry
12/6/1988
032
Chemistry
11/17/1987
030
Chemistry
11/17/1987
029
Chemistry
11/17/1987
028
Chemistry
11/17/1987
027
Chemistry
11/17/1987
025
Chemistry
11/17/1987
024
Chemistry
2/26/1986
023
Chemistry
2/27/1985
021
Chemistry
10/19/1981
000
Approval
Therapeutic Equivalents
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