YAOPHARMA CO LTD FDA Approval ANDA 073168

ANDA 073168

YAOPHARMA CO LTD

FDA Drug Application

Application #073168

Application Sponsors

ANDA 073168YAOPHARMA CO LTD

Marketing Status

Discontinued001

Application Products

001TABLET;ORAL40MG0VERAPAMIL HYDROCHLORIDEVERAPAMIL HYDROCHLORIDE

FDA Submissions

ORIG1AP1992-07-31
MANUF (CMC); Manufacturing (CMC)SUPPL2AP1994-01-24
MANUF (CMC); Manufacturing (CMC)SUPPL3AP1997-10-27
LABELING; LabelingSUPPL4AP1998-06-23
MANUF (CMC); Manufacturing (CMC)SUPPL5AP1999-05-05
MANUF (CMC); Manufacturing (CMC)SUPPL6AP2002-12-09
MANUF (CMC); Manufacturing (CMC)SUPPL7AP2002-12-16

Submissions Property Types

SUPPL1Null0
SUPPL2Null0
SUPPL3Null0
SUPPL5Null0
SUPPL6Null0
SUPPL7Null0

CDER Filings

YAOPHARMA CO LTD
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 73168
            [companyName] => YAOPHARMA CO LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"VERAPAMIL HYDROCHLORIDE","activeIngredients":"VERAPAMIL HYDROCHLORIDE","strength":"40MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"VERAPAMIL HYDROCHLORIDE","submission":"VERAPAMIL HYDROCHLORIDE","actionType":"40MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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