DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
XYLOCAINE 1.5% W/ DEXTROSE 7.5%
FDA Application No:
(NDA) 016297
Active Ingredient(s):
LIDOCAINE HYDROCHLORIDE
Company:
ABRAXIS BIOSCIENCE
Label History
Labels are not available on this site for XYLOCAINE 1.5 W DEXTROSE 7.5, (NDA) 016297
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/18/1993
012
Manufacturing Change or Addition
5/31/1988
011
Labeling Revision
9/16/1987
010
Manufacturing Change or Addition
9/19/1984
009
Practioner Draft Labeling
6/20/1984
008
Manufacturing Change or Addition
3/25/1982
007
Control Supplement
8/29/1979
006
Labeling Revision
5/15/1978
004
Expiration Date Change
6/28/1977
003
Labeling Revision
12/30/1974
001
Labeling Revision
11/4/1968
000
Approval
There are no Therapeutic Equivalents
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