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) 018579
Active Ingredient(s):
FUROSEMIDE
Company:
LUITPOLD
Label History
Labels are not available on this site for FUROSEMIDE, (NDA) 018579
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/27/2002
023
Packaging Addition
6/27/2002
022
Labeling
6/27/2002
021
Microbiology
7/15/2002
020
Facility Addition
12/4/2000
019
Expiration Date Change
12/4/2000
018
Control Supplement
12/4/2000
017
Supplier Addition
5/21/1997
016
Labeling
7/8/1997
015
Chemistry
2/28/1996
014
Chemistry
6/7/1993
013
Labeling in Effect
12/29/1992
012
Chemistry
4/14/1992
011
Labeling
8/22/1991
010
Labeling
8/15/1989
009
Chemistry
8/15/1989
008
Chemistry
8/15/1989
007
Chemistry
10/7/1988
006
Labeling
2/14/1989
004
Chemistry
11/30/1983
000
Approval
Therapeutic Equivalents
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