DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
UNIPEN
FDA Application No:
(NDA) 050462
Active Ingredient(s):
NAFCILLIN SODIUM
Company:
WYETH AYERST
Label History
Labels are not available on this site for UNIPEN, (NDA) 050462
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/3/1982
021
Control Supplement
9/30/1980
019
Labeling Revision
4/24/1978
018
Control Supplement
12/22/1977
017
Labeling Revision
6/2/1977
016
Labeling Revision
4/21/1976
015
Labeling Revision
3/23/1975
014
Labeling Revision
8/19/1975
013
Labeling Revision
11/22/1976
011
Labeling Revision
4/11/1974
010
Control Supplement
3/8/1974
009
Package Change
3/8/1974
008
Labeling Revision
4/10/1991
007
Labeling Revision
9/28/1987
006
Labeling Revision
1/20/1987
005
Package Change
12/5/1986
004
Labeling Revision
11/21/1986
003
Control Supplement
12/28/1982
002
Labeling Revision
12/14/1982
001
Control Supplement
10/16/1973
000
Approval
There are no Therapeutic Equivalents
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