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) 083501
Active Ingredient(s):
PROPOXYPHENE HYDROCHLORIDE
Company:
WEST WARD
Label History
Labels are not available on this site for PROPOXYPHENE HYDROCHLORIDE, (ANDA) 083501
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/8/2002
040
Expiration Date Change
8/8/2002
039
Packaging Addition
8/8/2002
038
Control Supplement
8/8/2002
037
Manufacturing Revision
8/8/2002
036
Supplier Addition
3/12/1999
035
Chemistry
10/1/1998
034
Chemistry
9/30/1993
033
Chemistry
10/7/1992
032
Labeling
7/22/1992
031
Labeling
3/19/1991
030
Chemistry
4/6/1988
029
Chemistry
3/3/1988
028
Chemistry
3/3/1988
027
Chemistry
3/3/1988
026
Chemistry
3/3/1988
025
Chemistry
3/3/1988
024
Chemistry
2/2/1989
023
Labeling
1/11/1991
022
Labeling
1/11/1991
021
Chemistry
1/11/1991
020
Chemistry
1/11/1991
019
Chemistry
2/21/1989
017
Chemistry
6/20/1973
000
Approval
Therapeutic Equivalents
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