Documents
Application Sponsors
ANDA 077937 | SUN PHARM INDS INC | |
Marketing Status
Discontinued | 001 |
Discontinued | 002 |
Application Products
001 | TABLET;ORAL | 7.5MG | 0 | MELOXICAM | MELOXICAM |
002 | TABLET;ORAL | 15MG | 0 | MELOXICAM | MELOXICAM |
FDA Submissions
| ORIG | 1 | AP | 2006-07-19 | |
LABELING; Labeling | SUPPL | 3 | AP | 2007-08-09 | |
LABELING; Labeling | SUPPL | 4 | AP | 2008-02-29 | |
LABELING; Labeling | SUPPL | 9 | AP | 2008-12-31 | |
CDER Filings
SUN PHARM INDS INC
cder:Array
(
[0] => Array
(
[ApplNo] => 77937
[companyName] => SUN PHARM INDS INC
[docInserts] => ["",""]
[products] => [{"drugName":"MELOXICAM","activeIngredients":"MELOXICAM","strength":"7.5MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"MELOXICAM","activeIngredients":"MELOXICAM","strength":"15MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"MELOXICAM","submission":"MELOXICAM","actionType":"7.5MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"MELOXICAM","submission":"MELOXICAM","actionType":"15MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)