DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ALLOPURINOL
FDA Application No:
(NDA) 018832
Active Ingredient(s):
ALLOPURINOL
Company:
WATSON LABS
Label History
Labels are not available on this site for ALLOPURINOL, (NDA) 018832
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/14/2002
027
Control Supplement
4/25/2001
026
Control Supplement
2/5/2001
025
Control Supplement
3/27/1998
022
Chemistry
3/27/1998
021
Chemistry
7/30/1993
017
Chemistry in Effect
1/28/1991
016
Chemistry
5/31/1991
015
Chemistry
6/29/1990
014
Chemistry
7/7/1988
013
Chemistry
7/7/1988
012
Chemistry
12/17/1987
011
Chemistry
12/17/1987
010
Chemistry
12/17/1987
009
Chemistry
3/12/1987
008
Chemistry
9/11/1985
005
Chemistry
3/28/1985
004
Chemistry
3/28/1985
003
Chemistry
6/28/1985
002
Chemistry
9/28/1984
000
Approval
Therapeutic Equivalents
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