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) 070443
Active Ingredient(s):
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Company:
SANDOZ
Label History
Labels are not available on this site for PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN, (ANDA) 070443
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/15/2001
020
Control Supplement
9/23/1996
019
Chemistry
11/8/1995
018
Chemistry
3/24/1999
017
Chemistry
6/7/1994
016
Chemistry
11/15/1989
015
Labeling in Effect
7/21/1988
014
Labeling
1/11/1989
013
Chemistry
7/9/1987
011
Chemistry
7/9/1987
010
Chemistry
7/9/1987
009
Chemistry
4/8/1987
008
Chemistry
4/8/1987
007
Chemistry
4/8/1987
006
Chemistry
2/20/1987
005
Chemistry
1/6/1987
004
Chemistry
9/29/1986
002
Chemistry
9/29/1986
001
Chemistry
1/23/1987
000
Approval
There are no Therapeutic Equivalents
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