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) 080269
Active Ingredient(s):
PROPOXYPHENE HYDROCHLORIDE
Company:
PAR PHARM
Label History
Labels are not available on this site for PROPOXYPHENE HYDROCHLORIDE, (ANDA) 080269
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/29/2002
109
Facility Addition
3/12/2002
108
Facility Addition
9/21/2000
107
Control Supplement
9/21/2000
106
Facility Addition
4/12/2000
105
Facility Addition
1/28/2000
104
Facility Addition
11/23/1999
103
Facility Addition
8/20/1999
102
Chemistry
12/23/1998
101
Chemistry
12/9/1998
100
Chemistry
5/30/1997
099
Chemistry
10/29/1992
098
Chemistry in Effect
9/4/1992
097
Chemistry in Effect
2/26/1992
096
Labeling
6/11/1987
094
Chemistry
2/18/1987
093
Chemistry
2/18/1987
092
Chemistry
11/30/1971
000
Approval
Therapeutic Equivalents
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