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) 074119
Active Ingredient(s):
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Company:
TEVA
Label History
Labels are not available on this site for PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN, (ANDA) 074119
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/13/2002
023
Labeling
8/13/2002
022
Control Supplement
8/13/2002
021
Manufacturing Revision
7/7/2000
020
Facility Addition
10/22/1999
019
Labeling
3/9/1998
018
Chemistry
4/1/1997
017
Labeling
1/29/1997
016
Chemistry
12/13/1996
015
Chemistry
6/30/1997
014
Chemistry
8/16/1996
013
Chemistry
6/6/1996
012
Chemistry
5/6/1996
011
Chemistry
10/20/1995
010
Chemistry
10/3/1995
009
Chemistry
10/3/1995
008
Chemistry
10/3/1995
007
Chemistry
10/3/1995
006
Chemistry
10/3/1995
005
Chemistry
10/3/1995
004
Chemistry
2/12/1996
003
Labeling
11/17/1995
002
Chemistry
10/20/1995
001
Chemistry
12/19/1994
000
Approval
There are no Therapeutic Equivalents
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