Documents
Application Sponsors
ANDA 075887 | UPSHER SMITH LABS | |
Marketing Status
Discontinued | 001 |
Discontinued | 002 |
Discontinued | 003 |
Application Products
001 | TABLET;ORAL | 25MG | 0 | FLUVOXAMINE MALEATE | FLUVOXAMINE MALEATE |
002 | TABLET;ORAL | 50MG | 0 | FLUVOXAMINE MALEATE | FLUVOXAMINE MALEATE |
003 | TABLET;ORAL | 100MG | 0 | FLUVOXAMINE MALEATE | FLUVOXAMINE MALEATE |
FDA Submissions
| ORIG | 1 | AP | 2001-01-05 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 2 | AP | 2001-11-26 | |
LABELING; Labeling | SUPPL | 7 | AP | 2003-08-29 | |
Submissions Property Types
CDER Filings
UPSHER SMITH LABS
cder:Array
(
[0] => Array
(
[ApplNo] => 75887
[companyName] => UPSHER SMITH LABS
[docInserts] => ["",""]
[products] => [{"drugName":"FLUVOXAMINE MALEATE","activeIngredients":"FLUVOXAMINE MALEATE","strength":"25MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"FLUVOXAMINE MALEATE","activeIngredients":"FLUVOXAMINE MALEATE","strength":"50MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"FLUVOXAMINE MALEATE","activeIngredients":"FLUVOXAMINE MALEATE","strength":"100MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"FLUVOXAMINE MALEATE","submission":"FLUVOXAMINE MALEATE","actionType":"25MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"FLUVOXAMINE MALEATE","submission":"FLUVOXAMINE MALEATE","actionType":"50MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"FLUVOXAMINE MALEATE","submission":"FLUVOXAMINE MALEATE","actionType":"100MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)