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:
(ANDA) 071379
Active Ingredient(s):
FUROSEMIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for FUROSEMIDE, (ANDA) 071379
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/7/2002
020
Facility Addition
8/31/2001
019
Control Supplement
11/10/1999
018
Package Change
12/11/1998
017
Labeling
6/23/1999
016
Chemistry
4/29/1996
015
Labeling
6/11/1993
014
Labeling
4/8/1993
013
Labeling
8/24/1992
012
Labeling
6/2/1992
011
Labeling in Effect
12/4/1990
010
Labeling
8/2/1990
009
Labeling in Effect
4/12/1990
008
Labeling
5/8/1990
007
Chemistry
5/8/1990
006
Chemistry
11/4/1988
005
Chemistry
6/20/1988
004
Chemistry
6/20/1988
003
Chemistry
6/20/1988
002
Chemistry
9/10/1987
001
Chemistry
1/2/1987
000
Approval
Therapeutic Equivalents
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