DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METOCLOPRAMIDE HYDROCHLORIDE
FDA Application No:
(ANDA) 070581
Active Ingredient(s):
METOCLOPRAMIDE HYDROCHLORIDE
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for METOCLOPRAMIDE HYDROCHLORIDE, (ANDA) 070581
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/23/2002
022
Labeling
11/2/2001
021
Control Supplement
2/1/2002
020
Labeling
5/26/2000
019
Control Supplement
11/24/1999
018
Labeling
1/27/2000
017
Package Change
1/18/1996
016
Chemistry
3/28/1991
015
Labeling
7/10/1991
014
Chemistry
11/1/1988
012
Labeling
11/23/1987
010
Chemistry
9/15/1986
009
Labeling
6/23/1987
006
Labeling
6/15/1987
005
Chemistry
6/15/1987
004
Chemistry
6/15/1987
003
Chemistry
11/25/1986
002
Chemistry
11/25/1986
001
Chemistry
10/17/1985
000
Approval
Therapeutic Equivalents
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