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) 071536
Active Ingredient(s):
METOCLOPRAMIDE HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for METOCLOPRAMIDE HYDROCHLORIDE, (ANDA) 071536
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/9/2002
020
Labeling
6/27/2002
017
Control Supplement
4/19/2002
016
Control Supplement
10/7/2002
015
Expiration Date Change
10/7/2002
014
Packaging Addition
10/7/2002
013
Control Supplement
10/7/2002
012
Labeling
5/16/2000
011
Facility Addition
4/11/2000
010
Labeling
5/16/2000
009
Facility Addition
12/5/1997
008
Chemistry
2/24/1997
007
Chemistry
1/16/1997
006
Chemistry
1/16/1997
005
Labeling
1/16/1997
004
Chemistry New Strength
1/16/1996
003
Chemistry
6/22/1995
002
Chemistry
1/12/1994
001
Chemistry
4/28/1993
000
Approval
Therapeutic Equivalents
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