DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NEBCIN
FDA Application No:
(NDA) 050477
Active Ingredient(s):
TOBRAMYCIN SULFATE
Company:
LILLY
Label History
Labels are not available on this site for NEBCIN, (NDA) 050477
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/2/2003
024
Labeling Revision
Letter
3/4/1999
023
Control Supplement
10/1/1997
021
Patient Population Altered
4/3/1997
020
Control Supplement
10/18/1995
019
Manufacturing Change or Addition
3/19/1997
018
Labeling Revision
5/13/1997
017
Labeling Revision
4/1/1993
016
Labeling Revision
8/6/1992
015
Labeling Revision
5/28/1980
014
Package Change
6/2/1976
013
Labeling Revision
2/23/1976
012
Labeling Revision
1/13/1976
011
Package Change
9/3/1975
010
New Dosage Regimen
7/30/1975
009
Labeling Revision
10/28/1991
008
Package Change
10/28/1991
007
Labeling Revision
7/21/1987
006
Labeling Revision
4/2/1987
005
Labeling Revision
3/5/1987
004
Control Supplement
11/4/1985
003
Labeling Revision
9/28/1984
002
Control Supplement
2/24/1984
001
Control Supplement
6/11/1975
000
Approval
There are no Therapeutic Equivalents
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