ANDA 072922

PLIVA

FDA Drug Application

Application #072922

Application Sponsors

ANDA 072922

PLIVA

Marketing Status

• Discontinued: 001

Application Products

001

TABLET, EXTENDED RELEASE;ORAL

240MG

0

VERAPAMIL HYDROCHLORIDE

VERAPAMIL HYDROCHLORIDE

FDA Submissions

ORIG

1

AP

1996-03-01

CDER Filings

PLIVA

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 72922
            [companyName] => PLIVA
            [docInserts] => ["",""]
            [products] => [{"drugName":"VERAPAMIL HYDROCHLORIDE","activeIngredients":"VERAPAMIL HYDROCHLORIDE","strength":"240MG","dosageForm":"TABLET, EXTENDED RELEASE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"VERAPAMIL HYDROCHLORIDE","submission":"VERAPAMIL HYDROCHLORIDE","actionType":"240MG","submissionClassification":"TABLET, EXTENDED RELEASE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)