DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROPOXYPHENE HYDROCHLORIDE
FDA Application No:
(ANDA) 088615
Active Ingredient(s):
PROPOXYPHENE HYDROCHLORIDE
Company:
TEVA
Label History
Labels are not available on this site for PROPOXYPHENE HYDROCHLORIDE, (ANDA) 088615
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/7/2000
024
Facility Addition
3/9/1998
023
Chemistry
12/11/1996
022
Chemistry
4/22/1997
021
Labeling
1/25/1996
020
Chemistry
1/25/1996
019
Chemistry
1/25/1996
018
Chemistry
7/17/1996
017
Labeling
7/17/1996
016
Chemistry
7/17/1996
015
Chemistry
10/31/1995
014
Labeling
3/2/1995
013
Chemistry
1/26/1994
012
Chemistry
1/26/1994
011
Chemistry
1/26/1994
010
Chemistry
1/26/1994
009
Chemistry
1/26/1994
008
Chemistry
1/26/1994
007
Chemistry
4/1/1993
006
Chemistry
5/25/1993
005
Chemistry
5/25/1993
004
Chemistry
7/30/1993
003
Chemistry
6/12/1989
002
Labeling
10/22/1984
000
Approval
Therapeutic Equivalents
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