DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
LIDOCAINE HYDROCHLORIDE
FDA Application No:
(ANDA) 087881
Active Ingredient(s):
LIDOCAINE HYDROCHLORIDE
Company:
MORTON GROVE
Label History
Labels are not available on this site for LIDOCAINE HYDROCHLORIDE, (ANDA) 087881
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/13/2002
011
Control Supplement
4/15/2002
010
Labeling
2/16/1994
009
Labeling
5/28/1992
008
Labeling
9/6/1989
007
Labeling
5/14/1987
003
Chemistry
10/6/1983
001
Chemistry
11/18/1982
000
Approval
Therapeutic Equivalents
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