DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CEDAX
FDA Application No:
(NDA) 050686
Active Ingredient(s):
CEFTIBUTEN DIHYDRATE
Company:
SHIONOGI
Label History
Labels are not available on this site for CEDAX, (NDA) 050686
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/4/2001
011
Package Change
5/19/2000
009
Labeling Revision
10/2/1998
008
Control Supplement
6/15/1998
007
Labeling Revision
2/16/1999
006
Labeling Revision
3/3/1998
005
Package Change
9/3/1997
004
Manufacturing Change or Addition
9/10/1996
003
Control Supplement
5/21/1997
002
Labeling Revision
10/9/1996
001
Labeling Revision
12/20/1995
000
Approval
There are no Therapeutic Equivalents
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