ANDA 070949

MORTON GROVE

FDA Drug Application

Application #070949

Application Sponsors

ANDA 070949

MORTON GROVE

Marketing Status

• Discontinued: 001

Application Products

001

SOLUTION;ORAL

EQ 5MG BASE/5ML

0

METOCLOPRAMIDE HYDROCHLORIDE

METOCLOPRAMIDE HYDROCHLORIDE

FDA Submissions

	ORIG	1	AP	1993-06-28
LABELING; Labeling	SUPPL	5	AP	1989-05-25
LABELING; Labeling	SUPPL	6	AP	1991-11-07
LABELING; Labeling	SUPPL	7	AP	1991-03-19
LABELING; Labeling	SUPPL	8	AP	1991-05-31
LABELING; Labeling	SUPPL	9	AP	1993-06-08
LABELING; Labeling	SUPPL	10	AP	1993-11-24
LABELING; Labeling	SUPPL	11	AP	1996-03-01

CDER Filings

MORTON GROVE

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 70949
            [companyName] => MORTON GROVE
            [docInserts] => ["",""]
            [products] => [{"drugName":"METOCLOPRAMIDE HYDROCHLORIDE","activeIngredients":"METOCLOPRAMIDE HYDROCHLORIDE","strength":"EQ 5MG BASE\/5ML","dosageForm":"SOLUTION;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"METOCLOPRAMIDE HYDROCHLORIDE","submission":"METOCLOPRAMIDE HYDROCHLORIDE","actionType":"EQ 5MG BASE\/5ML","submissionClassification":"SOLUTION;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)