IMPAX LABS FDA Approval ANDA 084928

ANDA 084928

IMPAX LABS

FDA Drug Application

Application #084928

Application Sponsors

ANDA 084928IMPAX LABS

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL750MG0METHOCARBAMOLMETHOCARBAMOL

FDA Submissions

ORIG1AP1976-08-20
MANUF (CMC); Manufacturing (CMC)SUPPL23AP1986-08-15
MANUF (CMC); Manufacturing (CMC)SUPPL24AP1986-08-15
MANUF (CMC); Manufacturing (CMC)SUPPL25AP1987-07-02
MANUF (CMC); Manufacturing (CMC)SUPPL26AP1988-04-18
MANUF (CMC); Manufacturing (CMC)SUPPL27AP1987-09-03
MANUF (CMC); Manufacturing (CMC)SUPPL28AP1987-11-14
LABELING; LabelingSUPPL29AP1988-06-10
LABELING; LabelingSUPPL30AP1988-12-19
LABELING; LabelingSUPPL31AP1989-09-28

Submissions Property Types

SUPPL23Null0
SUPPL24Null0
SUPPL25Null0
SUPPL26Null0
SUPPL27Null0
SUPPL28Null0

CDER Filings

IMPAX LABS
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 84928
            [companyName] => IMPAX LABS
            [docInserts] => ["",""]
            [products] => [{"drugName":"METHOCARBAMOL","activeIngredients":"METHOCARBAMOL","strength":"750MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"METHOCARBAMOL","submission":"METHOCARBAMOL","actionType":"750MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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