DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEFOXIN
FDA Application No:
(ANDA) 062757
Active Ingredient(s):
CEFOXITIN SODIUM
Company:
MERCK
Label History
Labels are not available on this site for MEFOXIN, (ANDA) 062757
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/30/2002
021
Package Change
6/4/2002
020
Facility Addition
6/4/2002
019
Control Supplement
12/6/2001
018
Manufacturing Revision
12/17/1999
017
Supplier Addition
7/11/1997
016
Labeling
8/22/2002
015
Labeling
5/8/1996
014
Chemistry
2/26/1996
013
Labeling
2/18/1999
012
Labeling
7/16/1996
011
Labeling
3/20/1995
010
Chemistry
2/26/1996
009
Labeling
7/11/1997
008
Labeling
3/10/1992
005
Chemistry in Effect
2/10/1992
003
Chemistry
2/10/1992
002
Labeling
1/8/1987
000
Approval
Therapeutic Equivalents
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