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) 070819
Active Ingredient(s):
METOCLOPRAMIDE HYDROCHLORIDE
Company:
TEVA
Label History
Labels are not available on this site for METOCLOPRAMIDE HYDROCHLORIDE, (ANDA) 070819
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/18/1998
022
Chemistry
5/13/1997
021
Chemistry
3/11/1996
020
Labeling
2/16/1995
019
Chemistry
9/6/1994
018
Chemistry
3/10/1994
017
Labeling
12/6/1993
016
Chemistry
9/21/1993
015
Labeling
3/18/1993
014
Labeling in Effect
6/2/1993
013
Chemistry
6/17/1992
012
Labeling
3/12/1991
011
Labeling
9/6/1990
009
Labeling
3/14/1989
008
Labeling
1/18/1989
007
Chemistry
6/6/1988
006
Chemistry
5/5/1988
005
Chemistry
9/30/1987
003
Chemistry
9/30/1987
002
Chemistry
10/26/1987
001
Chemistry
7/10/1987
000
Approval
Therapeutic Equivalents
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