DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
KEFLEX
FDA Application No:
(NDA) 050406
Active Ingredient(s):
CEPHALEXIN
Company:
MIDDLEBROOK PHARMS
Label History
Labels are not available on this site for KEFLEX, (NDA) 050406
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/15/1996
012
Labeling Revision
3/14/1996
011
Labeling Revision
2/13/1995
010
Labeling Revision
8/27/1992
008
Labeling Revision
4/10/1990
007
Labeling Revision
1/4/1971
000
Approval
Therapeutic Equivalents
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