DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEPERIDINE HYDROCHLORIDE
FDA Application No:
(ANDA) 088640
Active Ingredient(s):
MEPERIDINE HYDROCHLORIDE
Company:
BARR
Label History
Labels are not available on this site for MEPERIDINE HYDROCHLORIDE, (ANDA) 088640
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/9/2001
028
Control Supplement
7/9/2001
027
Facility Addition
10/30/2000
025
Control Supplement
12/21/1999
024
Facility Addition
5/20/1999
023
Chemistry
3/12/1999
022
Chemistry
12/1/1998
021
Chemistry
10/4/1996
020
Chemistry
10/4/1996
019
Chemistry
10/4/1996
018
Chemistry
10/4/1996
017
Chemistry
12/23/1994
016
Chemistry
3/2/1994
015
Labeling
4/3/1992
014
Chemistry
4/3/1992
012
Chemistry
5/8/1991
011
SBA
9/27/1991
011
Labeling
8/30/1991
010
Chemistry
8/30/1991
009
Chemistry
10/27/1989
008
Labeling
8/28/1989
007
Labeling
4/1/1987
004
Chemistry
5/2/1985
002
Chemistry
9/19/1984
000
Approval
Therapeutic Equivalents
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