DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SENSORCAINE
FDA Application No:
(NDA) 018304
Active Ingredient(s):
BUPIVACAINE HYDROCHLORIDE
Company:
ABRAXIS BIOSCIENCE
Label History
Labels are not available on this site for SENSORCAINE, (NDA) 018304
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/23/2002
033
Microbiology
3/8/2002
032
Microbiology
6/8/2001
031
Control Supplement
6/1/2001
030
Labeling
7/30/1999
029
Chemistry
4/14/1997
028
Chemistry
5/31/1996
027
Chemistry
10/14/1997
024
Chemistry
12/27/1994
023
Microbiology
9/11/1992
021
Chemistry
3/10/1993
020
Chemistry
5/8/1992
019
Chemistry
11/8/1991
018
Chemistry
8/27/1991
016
Labeling
8/1/1989
015
Chemistry
8/1/1989
014
Chemistry
10/27/1989
013
Chemistry
8/27/1991
012
Labeling
5/11/1988
011
Labeling
9/24/1987
009
Chemistry
12/30/1981
000
Approval
Therapeutic Equivalents
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