SPECGX LLC FDA Approval ANDA 040773

ANDA 040773

SPECGX LLC

FDA Drug Application

Application #040773

Application Sponsors

ANDA 040773SPECGX LLC

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL50MG0BENZPHETAMINE HYDROCHLORIDEBENZPHETAMINE HYDROCHLORIDE

FDA Submissions

ORIG1AP2007-04-25

Submissions Property Types

SUPPL1Null15

TE Codes

001PrescriptionAA

CDER Filings

SPECGX LLC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 40773
            [companyName] => SPECGX LLC
            [docInserts] => ["",""]
            [products] => [{"drugName":"BENZPHETAMINE HYDROCHLORIDE","activeIngredients":"BENZPHETAMINE HYDROCHLORIDE","strength":"50MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"BENZPHETAMINE HYDROCHLORIDE","submission":"BENZPHETAMINE HYDROCHLORIDE","actionType":"50MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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