DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
LAROTID
FDA Application No:
(ANDA) 062226
Active Ingredient(s):
AMOXICILLIN
Company:
GLAXOSMITHKLINE
Label History
Labels are not available on this site for LAROTID, (ANDA) 062226
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/9/2002
029
Control Supplement
8/22/2001
027
Labeling
5/31/2001
026
Control Supplement
6/8/1999
023
Labeling
4/20/1998
022
Chemistry
9/24/1997
021
Labeling
8/4/1998
020
Labeling
5/22/1995
018
Labeling in Effect
4/19/1993
017
Labeling in Effect
2/11/1992
016
Labeling
8/4/1998
015
Labeling
3/9/1993
014
Chemistry
6/23/1992
013
Chemistry
7/24/1989
012
Chemistry
11/27/1979
000
Approval
Therapeutic Equivalents
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