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) 089839
Active Ingredient(s):
QUINIDINE SULFATE
Company:
SANDOZ
Label History
Labels are not available on this site for QUINIDINE SULFATE, (ANDA) 089839
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/10/1996
006
Labeling
4/26/1995
005
Chemistry
6/26/1989
004
SBA
3/24/1989
003
Labeling
12/20/1988
001
Labeling
9/29/1988
000
Approval
Therapeutic Equivalents
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