DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CEFACLOR
FDA Application No:
(ANDA) 062205
Active Ingredient(s):
CEFACLOR
Company:
CEPH INTL
Label History
Labels are not available on this site for CEFACLOR, (ANDA) 062205
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/1/2000
051
Control Supplement
2/15/2000
050
Control Supplement
2/15/2000
049
Manufacturing Revision
12/23/1999
048
Facility Addition
8/30/1999
047
Labeling
3/3/1999
046
Chemistry
9/30/1998
045
Labeling
1/30/1998
043
Chemistry
10/23/1997
042
Labeling
4/1/1997
041
Labeling
6/10/1996
037
Labeling
4/7/1997
036
Chemistry
6/2/1994
035
Labeling in Effect
5/24/1994
032
Labeling
6/23/1992
031
Chemistry
6/23/1992
030
Chemistry
7/13/1994
029
Labeling
12/3/1992
028
Chemistry
8/19/1991
025
Chemistry
1/26/1989
016
Chemistry
7/28/1979
000
Approval
Therapeutic Equivalents
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