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) 081318
Active Ingredient(s):
LIDOCAINE HYDROCHLORIDE
Company:
TEVA PHARMS
Label History
Labels are not available on this site for LIDOCAINE HYDROCHLORIDE, (ANDA) 081318
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/14/2002
014
Control Supplement
2/14/2002
013
Facility Addition
10/31/2001
012
Facility Addition
10/31/2001
011
Facility Addition
10/31/2001
010
Facility Addition
1/23/2002
008
Facility Addition
2/26/2001
007
Facility Addition
3/23/1999
006
Chemistry
11/23/1998
005
Chemistry
7/15/1998
004
Chemistry
5/7/1998
003
Chemistry
5/24/1996
002
Chemistry
5/31/1996
001
Chemistry
4/29/1993
000
Approval
Therapeutic Equivalents
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