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) 081030
Active Ingredient(s):
QUINIDINE SULFATE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for QUINIDINE SULFATE, (ANDA) 081030
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/16/2001
011
Control Supplement
5/16/2000
010
Facility Addition
5/16/2000
009
Facility Addition
1/28/1999
008
Labeling
12/5/1997
007
Chemistry
2/24/1997
006
Chemistry
10/24/1996
005
Chemistry
3/25/1996
004
Labeling
6/22/1995
003
Chemistry
6/23/1994
002
Chemistry
1/12/1994
001
Chemistry
4/14/1989
000
Approval
Therapeutic Equivalents
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