BEXIMCO PHARMS USA FDA Approval ANDA 074542

ANDA 074542

BEXIMCO PHARMS USA

FDA Drug Application

Application #074542

Documents

Letter2000-05-10

Application Sponsors

ANDA 074542BEXIMCO PHARMS USA

Marketing Status

Discontinued001
Discontinued002

Application Products

001TABLET;ORAL5MG0GLIPIZIDEGLIPIZIDE
002TABLET;ORAL10MG0GLIPIZIDEGLIPIZIDE

FDA Submissions

ORIG1AP1995-06-20

Submissions Property Types

SUPPL1Null0

CDER Filings

BEXIMCO PHARMS USA
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 74542
            [companyName] => BEXIMCO PHARMS USA
            [docInserts] => ["",""]
            [products] => [{"drugName":"GLIPIZIDE","activeIngredients":"GLIPIZIDE","strength":"5MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"GLIPIZIDE","activeIngredients":"GLIPIZIDE","strength":"10MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"GLIPIZIDE","submission":"GLIPIZIDE","actionType":"5MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"GLIPIZIDE","submission":"GLIPIZIDE","actionType":"10MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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