Application Sponsors
ANDA 072514 | AUROLIFE PHARMA LLC | |
Marketing Status
Discontinued | 001 |
Discontinued | 002 |
Discontinued | 003 |
Application Products
001 | TABLET;ORAL | 15MG | 0 | CLORAZEPATE DIPOTASSIUM | CLORAZEPATE DIPOTASSIUM |
002 | TABLET;ORAL | 3.75MG | 0 | CLORAZEPATE DIPOTASSIUM | CLORAZEPATE DIPOTASSIUM |
003 | TABLET;ORAL | 7.5MG | 0 | CLORAZEPATE DIPOTASSIUM | CLORAZEPATE DIPOTASSIUM |
FDA Submissions
| ORIG | 1 | AP | 1990-05-11 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 2 | AP | 2000-01-10 | |
Submissions Property Types
CDER Filings
AUROLIFE PHARMA LLC
cder:Array
(
[0] => Array
(
[ApplNo] => 72514
[companyName] => AUROLIFE PHARMA LLC
[docInserts] => ["",""]
[products] => [{"drugName":"CLORAZEPATE DIPOTASSIUM","activeIngredients":"CLORAZEPATE DIPOTASSIUM","strength":"15MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"CLORAZEPATE DIPOTASSIUM","activeIngredients":"CLORAZEPATE DIPOTASSIUM","strength":"3.75MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"CLORAZEPATE DIPOTASSIUM","activeIngredients":"CLORAZEPATE DIPOTASSIUM","strength":"7.5MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"CLORAZEPATE DIPOTASSIUM","submission":"CLORAZEPATE DIPOTASSIUM","actionType":"15MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"CLORAZEPATE DIPOTASSIUM","submission":"CLORAZEPATE DIPOTASSIUM","actionType":"3.75MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"CLORAZEPATE DIPOTASSIUM","submission":"CLORAZEPATE DIPOTASSIUM","actionType":"7.5MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)