Documents
Application Sponsors
ANDA 075842 | BEXIMCO PHARMS USA | |
Marketing Status
Application Products
001 | TABLET;ORAL | 600MG | 0 | OXAPROZIN | OXAPROZIN |
FDA Submissions
CDER Filings
BEXIMCO PHARMS USA
cder:Array
(
[0] => Array
(
[ApplNo] => 75842
[companyName] => BEXIMCO PHARMS USA
[docInserts] => ["",""]
[products] => [{"drugName":"OXAPROZIN","activeIngredients":"OXAPROZIN","strength":"600MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"OXAPROZIN","submission":"OXAPROZIN","actionType":"600MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)