DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
UNASYN
FDA Application No:
(NDA) 050608
Active Ingredient(s):
AMPICILLIN SODIUM; SULBACTAM SODIUM
Company:
PFIZER
Label History
Labels are not available on this site for UNASYN, (NDA) 050608
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/19/2004
026
Labeling Revision
Letter
3/13/2002
025
Manufacturing Change or Addition
2/14/2001
024
Control Supplement
5/29/1998
023
Manufacturing Change or Addition
12/6/1996
021
Manufacturing Change or Addition
5/15/1996
020
Control Supplement
2/12/1997
019
Patient Population Altered
Review
12/10/1993
018
Package Change
11/5/1993
017
Labeling Revision
10/8/1992
016
Labeling Revision
3/24/1993
015
Manufacturing Change or Addition
5/8/1992
014
Control Supplement
4/23/1992
013
Control Supplement
1/2/1992
012
Control Supplement
3/27/1992
011
Labeling Revision
11/22/1991
009
Chemistry Generic
8/3/1989
007
Chemistry Generic
12/31/1986
000
Approval
There are no Therapeutic Equivalents
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