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) 087011
Active Ingredient(s):
QUINIDINE SULFATE
Company:
CLONMEL HLTHCARE
Label History
Labels are not available on this site for QUINIDINE SULFATE, (ANDA) 087011
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/25/1999
018
Labeling
3/12/1999
017
Chemistry
3/18/1996
016
Labeling
11/8/1994
015
Chemistry
8/6/1993
014
Chemistry
3/23/1989
013
Labeling
9/13/1985
010
Chemistry
3/26/1984
008
Chemistry
4/23/1982
005
Chemistry
4/23/1982
004
Chemistry
4/23/1982
003
Chemistry
4/23/1982
002
Chemistry
4/23/1982
001
Chemistry
8/29/1979
000
Approval
Therapeutic Equivalents
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