DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DIAMOX
FDA Application No:
(NDA) 008943
Active Ingredient(s):
ACETAZOLAMIDE
Company:
DURAMED PHARMS BARR
Label History
Labels are not available on this site for DIAMOX, (NDA) 008943
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/5/1999
048
Package Change
2/14/1991
047
Control Supplement
11/28/1990
046
Labeling Revision
4/23/1990
045
Control Supplement
1/24/1990
044
Labeling Revision
12/6/1989
043
Labeling Revision
7/21/1988
042
Expiration Date Change
6/22/1988
041
Labeling Revision
8/11/1987
040
Labeling Revision
6/16/1987
039
Control Supplement
10/6/1987
038
Control Supplement
3/3/1987
037
Labeling Revision
3/21/1986
036
Labeling Revision
5/13/1985
035
Labeling Revision
9/25/1984
034
Control Supplement
2/22/1984
033
Formulation Revision
9/29/1982
032
Control Supplement
4/2/1982
031
Package Change
6/12/1981
030
Formulation Revision
12/17/1980
029
Formulation Revision
12/17/1980
028
Formulation Revision
12/17/1980
027
Control Supplement
8/30/1979
026
Formulation Revision
2/14/1984
025
Control Supplement
7/31/1979
024
Control Supplement
10/2/1978
023
Labeling Revision
4/7/1978
022
Control Supplement
4/3/1978
021
Formulation Revision
1/9/1978
020
Control Supplement
6/29/1977
019
Control Supplement
6/29/1977
018
Formulation Revision
6/6/1977
017
Expiration Date Change
1/28/1977
015
Expiration Date Change
1/28/1977
013
Formulation Revision
7/27/1953
000
Approval
There are no Therapeutic Equivalents
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