Application Sponsors
| ANDA 084756 | LANNETT CO INC | |
Marketing Status
| Discontinued | 001 |
| Discontinued | 002 |
Application Products
| 001 | TABLET;ORAL | 750MG | 0 | METHOCARBAMOL | METHOCARBAMOL |
| 002 | TABLET;ORAL | 500MG | 0 | METHOCARBAMOL | METHOCARBAMOL |
FDA Submissions
| ORIG | 1 | AP | 1976-11-23 | |
| MANUF (CMC); Manufacturing (CMC) | SUPPL | 3 | AP | 1983-07-06 | |
| MANUF (CMC); Manufacturing (CMC) | SUPPL | 4 | AP | 2000-08-10 | |
| MANUF (CMC); Manufacturing (CMC) | SUPPL | 5 | AP | 2003-05-31 | |
| MANUF (CMC); Manufacturing (CMC) | SUPPL | 6 | AP | 2003-03-31 | |
| LABELING; Labeling | SUPPL | 7 | AP | 2003-03-31 | |
| LABELING; Labeling | SUPPL | 11 | AP | 2007-11-01 | |
Submissions Property Types
| SUPPL | 3 | Null | 0 |
| SUPPL | 4 | Null | 0 |
| SUPPL | 5 | Null | 0 |
| SUPPL | 6 | Null | 0 |
CDER Filings
LANNETT CO INC
cder:Array
(
[0] => Array
(
[ApplNo] => 84756
[companyName] => LANNETT CO INC
[docInserts] => ["",""]
[products] => [{"drugName":"METHOCARBAMOL","activeIngredients":"METHOCARBAMOL","strength":"750MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"METHOCARBAMOL","activeIngredients":"METHOCARBAMOL","strength":"500MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"METHOCARBAMOL","submission":"METHOCARBAMOL","actionType":"750MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"METHOCARBAMOL","submission":"METHOCARBAMOL","actionType":"500MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)