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) 084631
Active Ingredient(s):
QUINIDINE SULFATE
Company:
SANDOZ
Label History
Labels are not available on this site for QUINIDINE SULFATE, (ANDA) 084631
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/2/2000
018
Facility Addition
2/18/1999
017
Labeling
9/3/1996
016
Labeling
10/29/1992
015
Labeling in Effect
2/28/1995
014
Labeling
2/28/1995
013
Chemistry
2/5/1988
012
Labeling
3/12/1985
009
Chemistry
10/25/1983
007
Chemistry
10/25/1983
006
Chemistry
6/18/1982
001
Chemistry
11/24/1976
000
Approval
Therapeutic Equivalents
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