Application Sponsors
ANDA 075844 | SUN PHARM INDS INC | |
Marketing Status
Application Products
001 | TABLET;ORAL | 600MG | 0 | OXAPROZIN | OXAPROZIN |
FDA Submissions
| ORIG | 1 | AP | 2002-01-03 | |
LABELING; Labeling | SUPPL | 6 | AP | 2003-03-21 | |
LABELING; Labeling | SUPPL | 8 | AP | 2006-02-07 | |
LABELING; Labeling | SUPPL | 9 | AP | 2006-06-08 | |
LABELING; Labeling | SUPPL | 10 | AP | 2007-06-19 | |
LABELING; Labeling | SUPPL | 11 | AP | 2007-08-09 | |
Submissions Property Types
CDER Filings
SUN PHARM INDS INC
cder:Array
(
[0] => Array
(
[ApplNo] => 75844
[companyName] => SUN PHARM INDS INC
[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
)
)