DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
QUINIDINE SULFATE
FDA Application No:
(ANDA) 083288
Active Ingredient(s):
QUINIDINE SULFATE
Company:
WATSON LABS
Label History
Labels are not available on this site for QUINIDINE SULFATE, (ANDA) 083288
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/25/2001
071
Control Supplement
3/9/1998
069
Chemistry
11/20/1997
068
Chemistry
6/10/1996
067
Labeling
9/15/1994
066
Chemistry
1/28/1991
065
Chemistry
8/7/1991
064
Chemistry
6/29/1990
063
Chemistry
7/13/1989
062
Labeling
4/25/1989
061
Labeling
12/7/1988
060
Labeling
5/6/1988
059
Chemistry
5/6/1988
058
Chemistry
5/6/1988
057
Chemistry
6/7/1985
055
Chemistry
6/7/1985
054
Chemistry
8/19/1985
053
Chemistry
8/19/1985
050
Chemistry
8/19/1985
049
Chemistry
1/24/1985
048
Chemistry
5/23/1983
045
Chemistry
5/23/1983
044
Chemistry
11/24/1976
000
Approval
Therapeutic Equivalents
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