ANDA 089573

ABBOTT

FDA Drug Application

Application #089573

Application Sponsors

ANDA 089573

ABBOTT

Marketing Status

• Discontinued: 001

Application Products

001

INJECTABLE;INJECTION

EQ 40MG BASE/VIAL

0

A-METHAPRED

METHYLPREDNISOLONE SODIUM SUCCINATE

FDA Submissions

	ORIG	1	AP	1991-02-22
MANUF (CMC); Manufacturing (CMC)	SUPPL	2	AP	2002-03-12

Submissions Property Types

ORIG	1	Null	0
SUPPL	2	Null	0

CDER Filings

ABBOTT

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 89573
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"A-METHAPRED","activeIngredients":"METHYLPREDNISOLONE SODIUM SUCCINATE","strength":"EQ 40MG BASE\/VIAL","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"A-METHAPRED","submission":"METHYLPREDNISOLONE SODIUM SUCCINATE","actionType":"EQ 40MG BASE\/VIAL","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)