ANDA 074672

MLV

FDA Drug Application

Application #074672

Application Sponsors

ANDA 074672

MLV

Marketing Status

• Discontinued: 001

Application Products

001

TABLET;ORAL

5MG

0

SELEGILINE HYDROCHLORIDE

SELEGILINE HYDROCHLORIDE

FDA Submissions

ORIG

1

AP

1997-04-01

Submissions Property Types

ORIG

1

Null

0

TE Codes

001

Prescription

AB

CDER Filings

I3 PHARMS

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 74672
            [companyName] => I3 PHARMS
            [docInserts] => ["",""]
            [products] => [{"drugName":"SELEGILINE HYDROCHLORIDE","activeIngredients":"SELEGILINE HYDROCHLORIDE","strength":"5MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"SELEGILINE HYDROCHLORIDE","submission":"SELEGILINE HYDROCHLORIDE","actionType":"5MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)