ANDA 087131

PARKE DAVIS

FDA Drug Application

Application #087131

Application Sponsors

ANDA 087131

PARKE DAVIS

Marketing Status

• Discontinued: 001

Application Products

001

TABLET;ORAL

0.025MG;2.5MG

0

DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

FDA Submissions

ORIG

1

AP

1981-07-17

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 87131
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)