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) 088072
Active Ingredient(s):
QUINIDINE SULFATE
Company:
SANDOZ
Label History
Labels are not available on this site for QUINIDINE SULFATE, (ANDA) 088072
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/2/2000
013
Facility Addition
2/18/1999
012
Labeling
9/3/1996
011
Labeling
10/29/1992
010
Labeling in Effect
11/8/1994
009
Chemistry
11/8/1994
008
Chemistry
6/16/1989
007
Labeling
2/7/1989
006
Chemistry
5/13/1985
002
Chemistry
9/26/1983
000
Approval
Therapeutic Equivalents
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