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) 070655
Active Ingredient(s):
FUROSEMIDE
Company:
MORTON GROVE
Label History
Labels are not available on this site for FUROSEMIDE, (ANDA) 070655
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/3/1997
010
Labeling
3/15/1996
009
Labeling
8/4/1994
008
Labeling in Effect
4/6/1992
007
Labeling
1/16/1992
006
Labeling
6/5/1991
005
Labeling
10/24/1990
004
Labeling
4/3/1990
003
Labeling
4/3/1990
002
Labeling
1/25/1989
001
Labeling
10/1/1987
000
Approval
Therapeutic Equivalents
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