DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
KEFUROX
FDA Application No:
(ANDA) 062591
Active Ingredient(s):
CEFUROXIME SODIUM
Company:
ACS DOBFAR
Label History
Labels are not available on this site for KEFUROX, (ANDA) 062591
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/12/2002
038
Labeling
11/12/2002
037
Labeling
11/12/2002
036
Labeling
11/12/2002
035
Labeling
9/4/2002
034
Microbiology
9/5/2001
033
Control Supplement
1/22/2001
032
Labeling
1/22/2001
031
Chemistry
1/22/2001
030
Chemistry
1/22/2001
029
Chemistry
1/20/1999
026
Labeling
1/20/1999
025
Chemistry
8/15/1996
024
Chemistry
8/15/1996
023
Labeling
8/15/1996
022
Chemistry
1/23/1997
020
Labeling
1/13/1997
019
Chemistry
1/23/1997
018
Chemistry
6/12/1992
016
Labeling
12/10/1991
015
Labeling
2/3/1994
011
Labeling
6/12/1992
010
Chemistry in Effect
1/10/1986
000
Approval
There are no Therapeutic Equivalents
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