ANDA 075174

YAOPHARMA CO LTD

FDA Drug Application

Application #075174

Documents

• Letter: 1998-06-22

Application Sponsors

ANDA 075174

YAOPHARMA CO LTD

Marketing Status

• Discontinued: 001
• Discontinued: 002

Application Products

001	TABLET;ORAL	1.5MG	0	GLYBURIDE (MICRONIZED)	GLYBURIDE
002	TABLET;ORAL	3MG	0	GLYBURIDE (MICRONIZED)	GLYBURIDE

FDA Submissions

ORIG

1

AP

1998-06-22

CDER Filings

YAOPHARMA CO LTD

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 75174
            [companyName] => YAOPHARMA CO LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"GLYBURIDE (MICRONIZED)","activeIngredients":"GLYBURIDE","strength":"1.5MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"GLYBURIDE (MICRONIZED)","activeIngredients":"GLYBURIDE","strength":"3MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"GLYBURIDE (MICRONIZED)","submission":"GLYBURIDE","actionType":"1.5MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"GLYBURIDE (MICRONIZED)","submission":"GLYBURIDE","actionType":"3MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)