DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DIABINESE
FDA Application No:
(NDA) 011641
Active Ingredient(s):
CHLORPROPAMIDE
Company:
PFIZER
Label History
Labels are not available on this site for DIABINESE, (NDA) 011641
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/4/2004
061
Labeling Revision
Letter
Review
5/16/2002
060
Labeling Revision
Letter
Review
12/15/1999
059
Package Change
5/16/2002
058
Labeling Revision
Letter
Review
11/24/1993
057
Manufacturing Change or Addition
1/28/1993
056
Control Supplement
5/12/1987
055
Labeling Revision
2/24/1987
054
Package Change
9/4/1984
053
Control Supplement
9/4/1984
052
Package Change
9/4/1984
051
Package Change
10/18/1984
050
Practioner Draft Labeling
5/28/1982
049
Control Supplement
3/3/1981
047
Package Change
2/24/1978
044
Labeling Revision
5/16/1978
043
Package Change
10/28/1958
000
Approval
Therapeutic Equivalents
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