DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
FDA Application No:
(ANDA) 070910
Active Ingredient(s):
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN, (ANDA) 070910
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/2/2001
030
Control Supplement
9/24/2001
029
Control Supplement
9/24/2001
028
Control Supplement
6/15/2001
027
Facility Addition
1/18/1996
026
Chemistry
3/25/1998
025
Chemistry
8/19/1994
024
Chemistry
9/14/1993
023
Chemistry
8/20/1997
022
Chemistry
1/11/1991
021
Labeling
6/14/1990
019
Chemistry in Effect
6/14/1990
018
Chemistry in Effect
6/14/1990
017
Chemistry in Effect
9/11/1989
016
SBA
6/14/1990
016
Chemistry in Effect
9/11/1989
015
SBA
6/14/1990
015
Labeling in Effect
6/1/1989
014
SBA
10/5/1988
011
Labeling
8/23/1989
010
Labeling
4/8/1988
008
Chemistry
4/8/1988
007
Chemistry
9/16/1987
004
Chemistry
4/13/1987
002
Chemistry
4/13/1987
001
Chemistry
1/2/1987
000
Approval
There are no Therapeutic Equivalents
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