DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE
FDA Application No:
(NDA) 017584
Active Ingredient(s):
LIDOCAINE HYDROCHLORIDE
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for LIDOCAINE HYDROCHLORIDE PRESERVATIVE FREE, (NDA) 017584
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/13/1996
028
Labeling Revision
5/17/1993
027
Labeling Revision
12/19/1995
025
Control Supplement
12/19/1995
024
Control Supplement
8/23/1991
022
Manufacturing Change or Addition
4/7/1987
021
Control Supplement
8/5/1994
019
Labeling Revision
2/24/1986
018
Control Supplement
8/31/1984
017
Control Supplement
5/22/1986
016
Labeling Revision
2/14/1986
015
Practioner Draft Labeling
4/30/1985
014
Control Supplement
7/21/1982
013
Labeling Revision
12/8/1982
012
Control Supplement
2/5/1981
011
Control Supplement
1/9/1980
010
Labeling Revision
7/10/1979
009
Manufacturing Change or Addition
12/1/1977
008
Control Supplement
12/1/1977
007
Control Supplement
7/12/1977
006
Package Change
5/26/1978
005
Control Supplement
5/26/1978
004
Labeling Revision
10/29/1976
003
Labeling Revision
8/18/1976
002
Labeling Revision
6/8/1976
001
Control Supplement
3/26/1976
000
Approval
Therapeutic Equivalents
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