DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ERYTHROCIN
FDA Application No:
(NDA) 050609
Active Ingredient(s):
ERYTHROMYCIN LACTOBIONATE
Company:
HOSPIRA
Label History
Labels are not available on this site for ERYTHROCIN, (NDA) 050609
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/16/2004
019
Labeling Revision
Letter
12/13/2002
018
Expiration Date Change
8/29/2002
017
Control Supplement
3/20/2001
016
Control Supplement
5/23/2002
015
Labeling Revision
Letter
11/8/1999
014
Control Supplement
10/27/1997
011
Package Change
3/18/1996
010
Package Change
3/12/1993
009
Labeling Revision
8/24/1994
008
Labeling Revision
8/24/1994
007
Labeling Revision
12/5/1991
006
Chemistry Generic
9/21/1987
002
Labeling Revision
9/24/1986
000
Approval
Therapeutic Equivalents
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